Nanoscale structure and local mechanical properties of fiber-reinforced composites containing MWCNT-grafted hybrid glass fibers

Carbon nanotubes (CNTs) were grown from the surface of glass fibers by chemical vapor deposition, and these hybrid fibers were individually dispersed in an epoxy matrix to investigate the local composite structure and properties near the fiber surface. High-resolution transmission electron microscopy revealed the influence of infiltration and curing of a liquid epoxy precursor on the morphology of the CNT “forest” region, or region of high CNT density near the fiber surface. Subsequent image analysis highlighted the importance of spatially dependent volume fractions of CNTs in the matrix as a function of distance from the fiber surface, and nanoindentation was used to probe local mechanical properties in the CNT forest region, showing strong correlations between local stiffness and volume fraction. This work represents the first in situ measurements of local mechanical properties of the nano-structured matrix region in hybrid fiber-reinforced composites, providing a means of quantifying the reinforcement provided by the grafted nanofillers.     

Interfacial load transfer in carbon nanotube/ceramic microfiber hybrid polymer composites

Growing carbon nanotubes (CNTs) on the surface of fibers has the potential to modify fiber–matrix interfacial adhesion, enhance the composite delamination resistance, and possibly improve its toughness and any matrix-dominated elastic property as well. In the present work aligned CNTs were grown upon ceramic fibers (silica and alumina) by chemical vapor deposition (CVD) at temperatures of 650 °C and 750 °C. Continuously-monitored single fiber composite (SFC) fragmentation tests were performed on pristine as well as on CNT-grown fibers embedded in epoxy. The critical fragment length, fiber tensile strength at critical length, and interfacial shear strength were evaluated. Significant increases (up to 50%) are observed in the fiber tensile strength and in the interfacial adhesion (which was sometimes doubled) with all fiber types upon which CNTs are CVD-grown at 750 °C. We discuss the likely sources of these improvements as well as their implications.     

Carbon and glass hierarchical fibers: Influence of carbon nanotubes on tensile,flexural and impact properties of short fiber reinforced composites

Dense carbon nanotubes (CNTs) were grown uniformly on the surface of carbon fibers and glass fibers to create hierarchical fibers by use of floating catalyst chemical vapor deposition. Morphologies of the CNTs were investigated using scanning electronic microscope (SEM) and transmission electron microscope (TEM). Larger diameter dimension and distinct growing mechanism of nanotubes on glass fiber were revealed. Short carbon and glass fiber reinforced polypropylene composites were fabricated using the hierarchical fibers and compared with composites made using neat fibers. Tensile, flexural and impact properties of the composites were measured, which showed evident enhancement in all mechanical properties compared to neat short fiber composites. SEM micrographs of composite fracture surface demonstrated improved adhesion between CNT-coated fiber and the matrix. The enhanced mechanical properties of short fiber composites was attributed to the synergistic effects of CNTs in improving fiber–matrix interfacial properties as well as the CNTs acting as supplemental reinforcement in short fiber-composites.     

High performance polyimide composite films prepared by homogeneity reinforcement of electrospun nanofibers

Highly aligned polyimide (PI) and PI nanocomposite fibers containing carbon nanotubes (CNTs) were produced by electrospinning. Scanning electron microscopy showed the electrospun nanofibers were uniform and almost free of defects. Transmission electron microscopy indicated that the CNTs were finely dispersed and highly oriented along the CNT/PI nanofiber axis at a relatively low concentration. The as-prepared well-aligned electrospun nanofibers were then directly used as homogeneity reinforcement to enhance the tensile strength and toughness of PI films. The neat PI nanofiber reinforced PI films showed good transparency, decreased bulk density and significantly improved mechanical properties. Compared with neat PI film prepared by solution casting, the tensile strength and elongation at break for the PI film reinforced with 2 wt.% CNT/PI nanofibers were remarkably increased by 138% and 104%, respectively. The significant increases in the overall mechanical properties of the nanofibers reinforced polyimide films can be ascribed to good compatibility between the electrospun nanofibers and the matrix as well as high nanofiber orientation in the matrix. Our study demonstrates a good example for fabricating high performance and high toughness polyimide nanocomposites by using this facile homogeneity self-reinforcement method.     

Interfacial shear strength of a glass fiber/epoxy bonding in composites modified with carbon nanotubes

In recent years, carbon nanotubes (CNTs) grown on fibers have attracted a lot of interest as an additional reinforcing component in conventional fiber-reinforced composites to improve the properties of the fiber/matrix interface. Due to harsh growth conditions, the CNT-grafted fibers often exhibit degraded tensile properties. In the current study we explore an alternative approach to deliver CNTs to the fiber surface by dispersing CNTs in the fiber sizing formulation. This route takes advantage of the developed techniques for CNT dispersion in resins and introduces no damage to the fibers. We focus on unidirectional glass fiber/epoxy macro-composites where CNTs are introduced in three ways: (1) in the fiber sizing, (2) in the matrix and (3) in the fiber sizing and matrix simultaneously. Interfacial shear strength (IFSS) is investigated using single-fiber push-out microindentation. The results of the test reveal an increase of IFSS in all three cases. The maximum gain (over 90%) is achieved in the composite where CNTs are introduced solely in the fiber sizing.     

Development of slate fiber reinforced high density polyethylene composites for injection molding

During the last decade the use of fiber reinforced composite materials has consolidated as an attracting alternative to traditional materials due to an excellent balance between mechanical properties and lightweight. One drawback related to the use of inorganic fibers such as those derived from siliceous materials is the relative low compatibility with conventional organic polymer matrices. Surface treatments with coupling agents and the use of copolymers allow increasing fiber–matrix interactions which has a positive effect on overall properties of composites. In this research work we report the use of slate fiber treated with different coupling agents as reinforcement for high density polyethylene from sugarcane. A silane (propyltrimethoxy silane; PTMS) and a graft copolymer (polyethylene-graft-maleic anhydride; PE-g-MA) were used to improve fiber–matrix interactions on HDPE-slate fiber. The effect of the different compatibilizing systems and slate fiber content were evaluated by scanning electron microscopy (SEM), dynamic thermomechanical analysis (DTMA) as well as mechanical properties (tensile, flexural and impact). The results show that the use of silane coupling agents leads to higher fiber–matrix interactions which has a positive effect on overall mechanical properties. Interesting results are obtained for composites containing 30 wt.% slate fiber previously treated with propyltrimethoxy silane (PTMS) with an increase in tensile and flexural strength of about 16% and 18% respectively.     

Influence of carbon nanotube-polymeric compatibilizer masterbatches on morphological, thermal, mechanical, and tribological properties of polyethylene

Study was made of the effect of multiwall carbon nanotubes (MWCNTs) and polymeric compatibilizer on thermal, mechanical, and tribological properties of high density polyethylene (HDPE). The composites were prepared by melt mixing in two steps. Carbon nanotubes (CNTs) were melt mixed with maleic anhydride grafted polyethylene (PEgMA) as polymeric compatibilizer to produce a PEgMA-CNT masterbatch containing 20 wt% of CNTs. The masterbatch was then added to HDPE to prepare HDPE nanocomposites with CNT content of 2 or 6 wt%. The unmodified and modified (hydroxyl or amine groups) CNTs had similar effects on the properties of HDPE-PEgMA indicating that only non-covalent interactions were achieved between CNTs and matrix. According to SEM studies, single nanotubes and CNT agglomerates (size up to 1 μm) were present in all nanocomposites regardless of content or modification of CNTs. Addition of CNTs to HDPE-PEgMA increased decomposition temperature, but only slight changes were observed in crystallization temperature, crystallinity, melting temperature, and coefficient of linear thermal expansion (CLTE). Young’s modulus and tensile strength of matrix clearly increased, while elongation at break decreased. Measured values of Young’s moduli of HDPE-PEgMA-CNT composites were between the values of Young’s moduli for longitudinal (E₁₁) and transverse (E₂₂) direction predicted by Mori-Tanaka and Halpin-Tsai composite theories. Addition of CNTs to HDPE-PEgMA did not change the tribological properties of the matrix. Because of its higher crystallinity, PEgMA possessed significantly different properties from HDPE matrix: better mechanical properties, lower friction and wear, and lower CLTE in normal direction. Interestingly, the mechanical and tribological properties and CLTEs of HDPE-PEgMA-CNT composites lie between those of PEgMA and HDPE.     

Fracture behavior of nylon hybrid composites

Hybrid composite systems consisting of liquid crystalline polymer (LCP), short glass fibers and toughened nylon in varied ratios were studied. Dynamic mechanical results indicated that, elastomeric phase in toughened nylon 6,6 promoted a better compatibilization between nylon 6,6 and LCP in a hybrid system containing short glass fibers in comparison with one without glass fibers. Improved compatibility facilitated fibrillation of LCP phase in the skin region of the hybrid composite, thereby providing superior tensile strength. Without the presence of LCP, glass fiber reinforced toughened nylon 6,6 exhibited the least tensile strength. J-integral analysis and essential work of fracture (EWF) method were used to compare the fracture behavior of composites. Results showed that specific essential work of fracture were consistent with the critical J-integral. Matrices reinforced by LCP alone showed the best crack initiation and propagation toughnesses, followed by glass fiber reinforced and hybrid composites. The better compatibility between nylon 6,6 and LCP appeared to inhibit the interfacial debonding process, resulting in brittle fracture.     

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.     

Electron beam irradiation enhanced of Hibiscus cannabinus fiber strengthen polylactic acid composites

This paper reported the effects of increasing Hibiscus cannabinus fiber (also known as kenaf fiber) loading level on properties of electron beam irradiated polylactic acid/low density polyethylene (PLA/LDPE). PLA and LDPE were compounded with 5–20 parts per hundred resins (phr) of kenaf respectively to enhance mechanical properties. The compounded kenaf added PLA/LDPE samples were electron beam irradiated from 15 to 60 kGy. The physical properties of kenaf added PLA/LDPE samples were characterized using gel content, X-Ray diffraction and scanning electron microscopy analysis. The results showed that the increasing of irradiation dosages in PLA/LDPE have gradually increased the gel content and tensile strength due to the formation of crosslinking networks in polymer matrix. However, the higher loading level of kenaf and irradiation dosages could decrease the elongation at break of PLA/LDPE samples. This is due to the restriction of polymer chains mobility as resulted by the poor interfacial adhesion between polymer matrix and kenaf particles as well as the formation of crosslinking networks in polymer matrix limits the sliding of polymer chains. Meanwhile, the increasing of kenaf loading level also has gradually increased the crystallinity of PLA/LDPE matrix. It is concluded that the electron beam irradiation dosages and amount of kenaf fiber in PLA/LDPE matrix should be kept at maximum 45 kGy and 15 phr, respectively for better combination to enhance the properties of the composites.     

Mechanical properties of basalt fibers and their adhesion to polypropylene matrices

This work is aimed to study the mechanical properties of basalt fibers, and their adhesion to polypropylene (PP) matrices. Single filament tensile tests were used to calculate the strength of different types of fibers, characterized by different providers and surface treatment. Single fiber fragmentation tests (SFFT) were used to calculate the critical length of the fibers, in a homopolymer PP matrix and in a maleic anhydride modified PP matrix. It was shown that the tensile strength of the fibers is not significantly influenced by the origin or the surface treatment. Only fibers without any sizing show very reduced mechanical properties. On the other hand, the tensile strength was shown to be severely dependent on the filament length. Weibull theory was used in order to calculate the fitting parameters σ₀ and β, which were necessary in order to extrapolate the tensile strength to the critical length determined by SFFT. This allowed calculating the adhesion properties of the basalt fibers. It was shown that fiber–matrix adhesion is dependent on both the presence of sizing on the fiber surface, as well as on the modification of the matrix.     

Solid-state additive manufacturing for metallized optical fiber integration

The formation of smart, Metal Matrix Composite (MMC) structures through the use of solid-state Ultrasonic Additive Manufacturing (UAM) is currently hindered by the fragility of uncoated optical fibers under the required processing conditions. In this work, optical fibers equipped with metallic coatings were fully integrated into solid Aluminum matrices using processing parameter levels not previously possible. The mechanical performance of the resulting manufactured composite structure, as well as the functionality of the integrated fibers, was tested. Optical microscopy, Scanning Electron Microscopy (SEM) and Focused Ion Beam (FIB) analysis were used to characterize the interlaminar and fiber/matrix interfaces whilst mechanical peel testing was used to quantify bond strength. Via the integration of metallized optical fibers it was possible to increase the bond density by 20–22%, increase the composite mechanical strength by 12–29% and create a solid state bond between the metal matrix and fiber coating; whilst maintaining full fiber functionality.     

The effect of carbon nanotubes microstructures on reinforcing properties of SWNTs/alumina composite

Alumina reinforced with 1 wt% single-wall carbon nanotubes (SWNTs) was fabricated by hot-pressing. The fracture toughness of SWNTs/Al₂O₃ composite reaches 6.40 ± 0.3 MPa m^1/2, which is twice as high as that of unreinforced alumina. Nanoindentation introduced controlled cracks and the damage were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). SWNTs reinforcing mechanisms including CNT pullout, CNT fracture, CNT bridging and crack deflection were directly observed, and the relationship between carbon nanotubes microstructures in the matrix and mechanical properties was also discussed in detailed.     

Study of the energy absorption capabilities of laminated glass using carbon nanotubes

Laminated glass (LG) typically consists of two or more glass plies bonded together with a transparent thermoplastic elastomeric interlayer, often composed of polyvinyl butyral (PVB). This interlayer primarily serves as a means of preventing splintering and of absorbing energy upon blast/impact. This research attempted to enhance the impact resistance of LG by increasing PVB interlayer energy absorption by embedding carbon nanotubes (CNTs). Interlayers were formed by electrospinning aligned PVB fibers mat embedded with various concentrations of CNTs. Subsequently, the fiber mat was hot-pressed between two glass plies forming a composite film. The composite fibers were characterized using optical, SEM, and TEM microscopy. The mechanical and thermo-mechanical properties of fibers were determined by dynamic mechanical analysis (DMA), and the energy absorption capacities of the modified LGs were measured by applying the Charpy impact test of un-notched samples. A ∼ 30% increase in composite fiber (CNT 1.5 wt.%) strength was observed, along with a ∼ 70% increase in elastic modulus, measured at a strain rate of 0.1 min⁻¹, in comparison to CNT-free fibers. Increased CNT loading restricted the segmental motion of polymer macromolecules and provided the geometrical confinement effect to neighboring macromolecules in the nanoscale fiber. The energy absorption of a double-layered LG embedded with carbon nanotubes increased by nearly 341%, where experimental results demonstrated the role of the CNTs pull-out toughening mechanism. In parallel, transmission of visible light decreased by 60%.     

The dispersion of SWCNTs treated by dispersing agents in glass fiber reinforced polymer composites

It is an obstacle issue for carbon nanotubes (CNTs) particularly for single-wall carbon nanotubes (SWCNTs) with nano-level dispersion in fiber reinforced polymer matrix composites. In this paper, the dispersing agents such as Volan and BYK-9076 were employed to treat SWCNTs to improve their dispersion in the glass fiber/epoxy (GF/EP) composites. The dispersing results of SWCNTs in composites were observed by scanning electron microscopy (SEM). Then the glass transition temperature (T_g) of these kinds of composites with treated and untreated SWCNTs were obtained by dynamic mechanical thermal analysis (DMTA). Moreover, the flexural tests were performed on these composites. Based on the experiment results, the dispersion of SWCNTs was improved and the flexural property of SWCNTs/GF/EP composite was enhanced too.     

Effect of fiber diameter on the deformation behavior of self-assembled carbon nanotube reinforced electrospun Polyamide 6,6 fibers

High precision electrospinning technique was used to obtain self-assembled carbon nano-tube (CNT) reinforced polyamide (PA) 6,6 fibers. The reinforcement factors were critically evaluated with respect to the effects of fiber diameter and inclusion of CNTs. The average fiber diameter ranged from 240 to 1400 nm and the CNT contents were 0, 1 and 2.5 wt%. A sharp increase in modulus and strength of the fibers was demonstrated when the size of the fiber was decreased below ∼500 nm, which could be attributed to ordered arrangement of crystals and the spatial confinement effect of the fibers. Also, investigation of the deformation behavior of fibers as a function of CNT content revealed that tensile fiber modulus and strength improved significantly with increase of CNTs. Addition of CNTs restricted the segmental motion of polymer chains and provided the confinement effect to the neighboring molecules.     

Flexural and compression response of woven E-glass/polyester–CNF nanophased composites

A significant improvement in fiber reinforced polymeric composite (FRPC) materials can be obtained by incorporating a very small amount of nanofiller in the matrix material. In this work, an ultrasonic liquid processor was used to infuse carbon nanofiber (CNF) into the polyester matrix which was then mixed with catalyst using a mechanical agitator. Both conventional and CNF-filled glass-fiber reinforced polyester composites (GRPC) were fabricated using the vacuum assisted resin transfer molding (VARTM) process. Excellent dispersion of CNFs into the polyester resin was observed from the scanning electron microscopy (SEM) micrographs. Flexural and quasi-static tests were performed for investigating the mechanical responses. Fracture surface was examined using optical microscopy (OM) and SEM. Flexure tests performed on the conventional GRPC, 0.1–0.4 wt.% CNF-filled GRPC showed up to 49% and 31% increase in the flexural strength and modulus, respectively, compared to the conventional one with increasing loading of CNFs up to 0.2 wt.%. Similar trend was seen in quasi-static compression properties. SEM evaluation revealed relatively less damage in the tested fracture surfaces of the nanophased composites in terms of matrix failure, fiber breakage, matrix–fiber debonding, and delamination, compared to the conventional one. This might be the result of better interfacial interaction between matrix and fibers, due to the presence of CNFs.     

Biocomposites from Musa textilis and polypropylene: Evaluation of flexural properties and impact strength

Abaca (Musa textilis)-reinforced polypropylene composites have been prepared and their flexural mechanical properties studied. Due to their characteristic properties, M. textilis has a great economic importance and its fibers are used for specialty papers. Due to its high price and despite possessing very distinctive mechanical properties, to date abaca fibers had not been tested in fiber-reinforced composites. Analysis of materials prepared showed that, in spite of reduced interface adhesion, flexural properties of the PP composites increased linearly with fiber content up to 50 wt.%. Addition of a maleated polypropylene coupling agent still enhanced the stress transfer from the matrix to the reinforcement fiber. As a result, composites with improved flexural properties were obtained. The mechanical properties of matrix and reinforcing fiber were evaluated and used for modelling both the flexural strength and modulus of its composites. In addition, the impact strength of materials was evaluated. Comparison with mechanical properties of composites reinforced with fiberglass points out the potentiality of abaca-reinforced polypropylene composites as suitable substitutes in applications with low impact strength demands.     

Aligned ramie fiber reinforced arylated soy protein composites with improved properties

To enhance the strength, ramie fibers aligned in vertical (V), horizontal (H) as well as both vertical and horizontal (X) directions were used to reinforce soy protein materials (SC), coded as VSC, HSC and XSC. The soy protein isolate was arylated with 2,2-diphenyl-2-hydroxyethanoic acid through the process of “dip-coating”, coded as SC-B. The SC and SC-B composite films were characterized by Fourier transform infrared spectra, scanning electron microscopy, thermogravimetric analysis, dynamic mechanical thermal analysis, and tensile testing. Substantial improvement in the water uptake (from 100% to 25%) and the increased modulus (from 125 to 942 MPa) of the VSC-B composite were observed. This could be attributed to the formation of phase separation induced hydrophobic microparticles of DPHM on the surface of the SC-B films upon arylation, leading to the hydrophobicity. The thermal stability of the arylated composites increased compared to non-arylated ones. The VSC-B materials exhibited the highest water resistance and mechanical properties compared to HSC-B and XSC-B. Therefore, the arylation of SPI and alignment of the ramie fibers in the composites played an important role in the improvement of mechanical properties. This work provided a novel idea to improve the water resistance and modulus by reinforcing the protein matrix with natural fibers.     

In situ growth carbon nanotube reinforced SiCf/SiC composite

Carbon nanotube (CNT) reinforced SiC_f/SiC composite was prepared by in situ chemical vapor deposition (CVD) growth of CNTs on SiC fibers then following polymer impregnation pyrolysis (PIP) process. The nature of CNTs and the microstructure of the as prepared CNT-SiC_f/SiC composite were investigated. The mechanical properties of the as prepared CNT-SiC_f/SiC composite were measured. The results reveal that the in situ CVD growth of CNTs on SiC fibers remarkably promotes the mechanical properties of SiC_f/SiC composite. The secondly pull-out of CNTs from matrix during the pull-out of the SiC fibers from matrix consumes the deformation energies, resulting in promotion of the mechanical properties for composite.