Fabrication and mechanical/conductive properties of multi-walled carbon nanotube (MWNT) reinforced carbon matrix composites

Multi-walled carbon nanotube (MWNT) reinforced carbon matrix (MWNT/C) composites have been explored using mesophase pitch as carbon matrix precursor in the present work. Results show that carbon nanotubes (CNTs)can enhance the mechanical properties of carbon matrix significantly. The maximal increment of the bending strength and stiffness of the composites, compared with the carbon matrix, are 147% and 400%, respectively. Whereas the highest in-plane thermal conductivity of the composites is 86 W m^− 1 K^− 1 which much lower than that of carbon matrix (253 W m^− 1 K^− 1).At the same time the electrical resistivity of the composites is much higher than that of matrix. It is implicated that CNTs seem to play the role of thermal/electrical barrier in the composites. FSEM micrograph of the fracture surface for the composites shows that the presence of CNTs restrains the crystallite growth of carbon matrix, which is one of factors that improve mechanical properties and decrease the conductive properties of the composites. The defects and curved shape of CNTs are also the affecting factors on the conductive properties of the composites.     

Graphene foam/carbon nanotube/poly(dimethyl siloxane) composites for exceptional microwave shielding

Highly porous poly(dimethyl siloxane) (PDMS) composites containing cellular-structured microscale graphene foams (GFs) and conductive nanoscale carbon nanotubes (CNTs) are fabricated. The unique three-dimensional, multi-scale hybrid composites with inherent percolation and a high porosity of 90.8% present a remarkable electromagnetic interference shielding effectiveness (EMI SE) of ∼75 dB, a 200% enhancement against 25 dB of the composites made from GFs alone with the same graphene content and porosity. The corresponding specific EMI SE measured against the composite density is 833 dB cm³/g. These values are among the highest for all carbon filler/polymer composites reported thus far. Significant synergy arises from the hybrid reinforcement structure of the composites: the GFs drive the incident microwaves to be attenuated by dissipation of the currents induced by electromagnetic fields, while the CNTs greatly enhance the dissipation of surface currents by expanding the conductive networks and introducing numerous interfaces with the matrix.     

Preparation and characterization of biocompatible carbon electrodes

Electron transfer in microbial fuel cell and biosensors could be facilitated through high conductive materials with enhanced active surface area and appropriate redox potential suited to microbial metabolism. In the first strategy based on bulk doping, graphite/epoxy composite electrode (GECE) bulk was modified with six types of metal ion which were prepared through a wet impregnation procedure. In the second strategy, immobilization of redox dye on carbon cloth and graphite sheet was carried out using N,N′-dicyclohexylcarbodiimide for surface modification. Crystallinity, morphology, surface chemistry and electrochemical properties of all modified electrodes were investigated. Influence of redox behavior of electrodes suited to microbial metabolism and conducive to biofilm formation have been examined. It was observed that the Fe³⁺ doped GECE surfaces exhibited significantly high biofilm formation of 1.10(±0.18) × 10⁷ CFU/cm² as compared to other dopants. The microbial growth on the carbon cloth electrode and carbon fiber reinforced plate were found to be less (2.6(±0.97) × 10⁴, 4.8(±1.8) × 10³ CFU/cm² respectively) compared to GECEs.     

Advanced multifunctional properties of aligned carbon nanotube-epoxy thin film composites

Carbon nanotube (CNT)/epoxy composite films were successfully developed by a combination of layer-by-layer and vacuum-assisted resin transfer molding methods using directly chemical vapor deposition (CVD)-spun CNT plies. CNT fractions in the composite films were found to be dramatically enhanced as the number of CNT plies increased. The as-prepared CNT/epoxy composite films with 24.4 wt.% CNTs exhibited ~ 10 and ~ 5 times enhancements in their strength and Young's modulus, respectively, and high toughness of up to 6.39 × 10³ kJ/m³. Electrical conductivity reached 252.8 S/cm for the 20-ply CNT/epoxy films, which was 20 times higher over those of the CNT/epoxy composites obtained by conventional dispersion methods. This work proposed a route to fabricate high-CNT-fraction CNT/epoxy composites on a large scale. The high toughness of these CNT/epoxy composite films also makes them promising candidates as protective materials.     

Manufacture of a polymer-based carbon nanocomposite as bipolar plate of proton exchange membrane fuel cells

The aim of this paper is to prepare a polymer-based carbon nanocomposite reinforced by carbon fiber cloth (CF) to be utilized as bipolar plate of proton exchange membrane (PEM) fuel cell. For this purpose, some single, double, and triple-filler composites were manufactured by using phenolic resin as polymer (P) and graphite (G), carbon fiber (CF) and expanded graphite (EG) as fillers. The production method was compression-molding technique. The electrical conductivity, flexural strength, toughness, hardness, porosity, and hydrogen permeability tests were then measured to determine the mechanical and physical properties. A triple-filler composite containing 45 wt.% G, 10 wt.% CF, 5 wt.% EG, reinforced by a layer of CF cloth, was selected as composite bipolar plate. The electrical conductivity, thermal conductivity, and flexural strength of this composite were 74 S/cm, 9.6 W/m K, and 74 MPa, respectively, which are higher than the specified value by department of energy in USA (DOE). The composite bipolar plate used in the single fuel cell assembly showed a maximum power density 810 mW/cm². In this paper, a material selection was performed on the different materials of bipolar plates. It can be concluded that the composite bipolar plates are more suitable for high life time stationary applications.     

In situ preparation and mechanical properties of CNTs/MCMBs composites

By adding carbon nanotubes (CNTs) into medium temperature coal tar pitch, mesocarbon microbeads (MCMBs) were obtained via thermal condensation, then CNTs/MCMBs composites were in situ prepared using compression molding. The morphology, structure and mechanical properties of CNTs/MCMBs composites were characterized by optical microscope, digital camera, scanning electron microscope (SEM) and mechanical test machine. Results showed that CNTs were used as the nucleating agent and could inhibit the growth and coalescence of MCMBs. The optical textures of CNTs/MCMBs composites showed similar characteristics to the thermal condensation products from coal tar pitch with CNTs. The mass ratio of CNTs to coal tar pitch played an important role in the mechanical properties of CNTs/MCMBs composites. The density and bending strength of CNTs/MCMBs composite first increased and then decreased with the increase of the proportion of CNTs. When the proportion of CNTs was 5 wt%, the density of the composite reached the maximum (1.76 g/cm³). In addition, the bending strength of the composite reached the maximum (79.6 MPa) as adding 2 wt% CNTs into coal tar pitch.     

Preparation and characterization of poly(3-octylthiophene)/carbon fiber thermoelectric composite materials

Poly(3-alkylthiophene) (P3AT) with a high Seebeck coefficient has recently been reported. However, P3AT/inorganic conductive composites exhibit relatively poor thermoelectric performance because of their low electrical conductivity. In this work, carbon fiber sheets with a high electrical conductivity were chosen as the inorganic phase, and poly(3-octylthiophene)(P3OT)/carbon fiber composites were prepared by casting P3OT solution onto the carbon fiber sheets. The carbon fiber sheets incorporated into the composites can provide good electrical conductivity, and P3OT can provide a high Seebeck coefficient. The highest power factor of 7.05 μW m⁻¹ K⁻² was obtained for the composite with 50 wt% P3OT. This work suggests a promising method for preparing large-scale thermoelectric composites with excellent properties.     

Accelerated thermal ageing of epoxy resin and 3-D carbon fiber/epoxy braided composites

This paper reports the accelerated thermal ageing behaviors of pure epoxy resin and 3-D carbon fiber/epoxy braided composites. Specimens have been aged in air at 90 °C, 110 °C, 120 °C, 130 °C and 180 °C. Microscopy observations and attenuated total reflectance Fourier transform infrared spectrometry analyses revealed that the epoxy resin oxidative degradation only occurred within the surface regions. The surface oxidized layer protects inner resin from further oxidation. Both the resin degradation and resin stiffening caused by post-curing effects will influence the compression behaviors. For the braided composite, the matrix ageing is the main ageing mode at temperatures lower than glass transition temperatures (T_g) of the pure epoxy resin, while the fiber/matrix interface debonding could be observed at the temperatures higher than T_g, such as the temperature of 180 °C. The combination of matrix degradation and fiber/resin interface cracking leads to the continuous reduction of compressive behaviors.     

High conductive ethylene vinyl acetate composites filled with reduced graphene oxide and polyaniline

A conductive network composed of reduced graphene oxide (RGO) planes and polyaniline (PANI) chains was designed and fabricated by in situ polymerization of aniline monomer on the RGO planes. It was further used for fabrication of conductive composites with a polymer matrix–ethylene vinyl acetate (EVA). The composites achieve improved conductivity at a low filler loading although the host polymer–EVA–is of insulator. For instance, compared to the pure EVA polymer, the conductivity of the composite filled with 4.0 wt.% RGO and 8.0 wt.% PANI increases from 1.2 × 10^?14 S cm^?1 to 1.07 × 10^?1 S cm^?1. In addition, thermal stability of the composites is also enhanced by the filler loading.     

The effect of zirconium addition on the microstructure and properties of chopped carbon fiber/carbon composites

Carbon/carbon composites containing zirconium were prepared using chopped carbon fiber, mesophase pitch and Zr powder by the traditional process including molding, carbonization, densification and graphitization. The influence of Zr on the microstructure and properties of the composites were investigated. Results show that Zr can improve the interface bonding, promote more perfect and larger crystallites and enhance the conductive/mechanical properties of the composites. The high in-plane thermal conductivity of 464 W/(m K) and excellent bending strength of 83.6 MPa was obtained for a Zr content of 13.9 wt% at heat treatment temperature(HTT) of 2500 °C. However the conductive/mechanical properties of the composites decrease dramatically for an higher HTT of 3000 °C. SEM micrograph of the fracture surface for the composites shows that lower disorder crystallite arrangement of fiber and carbon matrix come into being in the composites during HTT of 3000 °C, which should be responsible for the low properties. Correlation between the content of Zr and the microstructure and properties are discussed.     

Thermal and mechanical properties of waste grass broom fiber-reinforced polyester composites

The main focus of this study is to utilize waste grass broom natural fibers as reinforcement and polyester resin as matrix for making partially biodegradable green composites. Thermal conductivity, specific heat capacity and thermal diffusivity of composites were investigated as a function of fiber content and temperature. The waste grass broom fiber has a tensile strength of 297.58 MPa, modulus of 18.28 GPa, and an effective density of 864 kg/m³. The volume fraction of fibers in the composites was varied from 0.163 to 0.358. Thermal conductivity of unidirectional composites was investigated experimentally by a guarded heat flow meter method. The results show that the thermal conductivity of composite decreased with increase in fiber content and the quite opposite trend was observed with respect to temperature. Moreover, the experimental results of thermal conductivity at different volume fractions were compared with two theoretical models. The specific heat capacity of the composite as measured by differential scanning calorimeter showed similar trend as that of the thermal conductivity. The variation in thermal diffusivity with respect to volume fraction of fiber and temperature was not so significant.The tensile strength and tensile modulus of the composites showed a maximum improvement of 222% and 173%, respectively over pure matrix. The work of fracture of the composites with maximum volume fraction of fibers was found to be 296 Jm⁻¹.     

Study on the mechanical properties,environmental effect,degradation characteristics and ionizing radiation effect on silk reinforced polypropylene/natural rubber composites

Natural silk fiber (20%) reinforced polypropylene (PP) composites were prepared by compression molding. Tensile strength, tensile modulus, bending strength, bending modulus, impact strength and hardness of the prepared composite were found 54.7 MPa, 1826.2 MPa, 58.3 MPa, 3750.7 MPa, 17.6 kJ/m² and 95 shore A, respectively. To improve the biodegradable character of the composite, natural rubber (NR) was blended (10%, 25%, 50% by weight) with PP. It was found that the mechanical properties of the composite decrease with increasing NR in PP (except IS which increased rather decreasing). Environmental effect on the composite and degradation in various media were investigated in this study. Gamma radiation was used to increase the mechanical properties of the prepared composites. Increase in TS and BS were maximum at 250 krad dose for silk fiber/PP, silk fiber/PP:NR (90:10), silk fiber/PP:NR (75:25) and silk fiber/PP:NR (50:50) composites.     

Effects of SiC interphase by chemical vapor deposition on the properties of C/ZrC composite prepared via precursor infiltration and pyrolysis route

Silicon carbide (SiC) interphase was introduced by chemical vapor deposition (CVD) process to prevent carbon fiber degradation and improve fiber–matrix interface bonding of C/ZrC composite prepared via precursor infiltration and pyrolysis (PIP) process. Moderate thickness of SiC interphase in fiber bundles could increase the density of the composite, but when the thickness of SiC interphase was over 0.5 μm, more close pores formed and the density of the composite decreased. The SiC interphase could protect carbon fiber effectively from carbo-thermal reduction, but could not enhance the mechanical properties of C/ZrC composite. The flexural strength and fracture toughness of C/ZrC composites with 0.05 μm thickness SiC layer were 252 MPa and 13.6 MPa m^1/2, and for those with 0.5 μm thickness SiC layer 240 MPa and 12.8 MPa m^1/2, both close to the value of the composite without SiC interphase (254 MPa and 14.5 MPa m^1/2), while those with 0.7 μm thickness SiC layer were only 191 MPa and 10.8 MPa m^1/2, respectively. Moderate content of SiC interphase could improve the ablation property of C/ZrC composites; however excessive content of SiC interphase would decrease the ablation property.     

Full-field shear analyses of sandwich core materials using Digital Image Correlation (DIC)

Mechanical properties and global stability of foam core sandwich structures are highly controlled by the shear response of the core material. In this work, we have studied the shear deformations of three common structural core materials with the aid of full-field optical analysis. The chosen core materials are namely extruded PET foam (ρ = 105 kg/m³, G_xz = 21 MPa,) and cross-linked PVC foam (ρ = 60 kg/m³, G_xz = 22 MPa) which have comparable shear properties, as well as Balsa wood with the lowest density commercially available (ρ = 94 kg/m³, G_xz = 106 MPa) as a reference core material. Both global and local shear strains in the core materials are calculated and graphically visualized. In the elastic region, foam cores showed more uniform deformations than Balsa. Yielding and shear failure of the two foam core materials were quite different. The PVC foam experienced a high local deformation under the load introduction bars, from which sub-interface shear failure initiated. The PET foam, in contrast, showed no sign of stress concentrations, resulting in a homogenous evolution of shear deformations in the mid-core regions. A comparison between the direct foam shear test and sandwich specimen bending suggested that the former method might not be capable of capturing a full picture of the in-service core shear response.     

Lightweight carbon-bonded carbon fiber composites with quasi-layered and network structure

Lightweight carbon-bonded carbon fiber (CBCF) composites were fabricated with chopped carbon fibers and dilute phenolic resin solution by pressure filtration, followed by carbonization at 1000 °C in argon. The as-prepared CBCF composites had a homogenous fiber network distribution in xy direction and quasi-layered structure in z direction. The pyrolytic carbon derived from phenolic resin was mainly accumulated at the intersections and surfaces of chopped carbon fibers. The composites possessed compressive strengths ranged from 0.93–6.63 MPa in xy direction to 0.30–2.01 MPa in z direction with a density of 0.162–0.381 g cm^− 3. The thermal conductivity increased from 0.314–0.505 to 0.139–0.368 Wm^− 1 K^− 1 in xy and z directions, respectively. The experimental results indicate that the CBCF composites prepared by this technique can significantly contribute to improve the thermal insulation and mechanical properties at high temperature.     

Gas sensitive vapor grown carbon nanofiber/polystyrene sensors

A new class of conductive composites with good gas sensitivity was fabricated by filling polystyrene with vapor grown carbon nanofibers (VGCNF). A solution mixing/solvent removal procedure was used. VGCNFs form conductive networks at fiber loadings above the percolation limit within the matrix. Greatly improved conductivity is achieved relative to the same volume fraction of carbon black addition when these fibers are distributed to give reasonably uniform dispersions in the matrix. The high aspect ratios of these fibers (∼70–250 nm diameters and 5–75 μm lengths) assist in forming low wt.% percolation thresholds (below 1 wt.% fiber). Excellent gas sensitivity with 10⁴–10⁵ times higher than the original resistance value in many saturated organic vapors and a maximum resistance response of about 1.1 × 10⁵ times exposure to saturated THF vapor at 6.25 wt.% of VGCNF in the polystyrene matrix was observed. The maximum resistance response declined from about 2.0 × 10⁵ times at 15 °C to about 3.4 × 10⁴ times at 55 °C. These composites exhibited stable and reusable gas sensitivity to THF vapor. Carbon black/polystyrene composites exhibit a negative vapor coefficient (NVC) upon swelling caused by filler redistribution. In contrast, VGCNF/polystyrene composites are more stable, with much smaller NVC values due to their high aspect ratios and reinforcing effects which stabilize electrical percolation pathways. Thus, VGCNF/organic polymer composites are good gas sensor candidates for detecting organic vapors.     

Scalable continuous growth of carbon nanotubes on moving fiber substrates

A process is developed to demonstrate the large scale production capability for creating carbon nanotube-based hybrid composite materials. A novel open-ended growth chamber and reel-to-reel scalable processing system is presented for the growth of carbon nanotubes (CNTs) directly on fiber substrates. This work focuses on the growth of the carbon nanotubes, characterization of the achievable CNT morphologies and measurements of the growth dynamics. This work demonstrates a continuous growth process capable of controlled CNT production on moving glass fiber substrates at throughput rates up to 40.7 mm s^?1 via maximum CNT growth rates of over 1.0 μm s^?1.     

Effects of thermal treatment on the mechanical properties of poly(p-phenylene benzobisoxazole) fiber reinforced phenolic resin composite materials

Thermal degradation behaviors of the poly(p-phenylene benzobisoxazole) (PBO) fiber and phenolic resin matrix were investigated. The unidirectional PBO fiber reinforced phenolic resin composite material laminates were fabricated and exposed in a muffle furnace of 300 °C, 550 °C, 700 °C, and 800 °C for 5 min, respectively, to study the effects of thermal treatment on mechanical properties of the composites. After undergone thermal treatments at 300 °C, 550 °C and 700 °C for 5 min, the flexural strength was reduced by 17%, 37% and 80%, respectively, the flexural modulus was decreased by 5%, 14% and 48%, respectively, and the interlaminar shear strength (ILSS) was lowered by 12%, 48% and 80%, respectively. Thermal treatment at 300 °C, the phenolic resin began to pyrolyze and shrink resulted in the irreversible damage of the composites. After 550 °C thermal treatment, the phenolic resin pyrolyzed mostly but the PBO fiber had no obvious pyrolyze, the interface had sever broken. After 700 °C thermal treatment, the phenolic resin formed amorphous carbonaceous and PBO fiber pyrolyzed mostly so the mechanical properties dropped dramatically. At being heated at 800 °C for 5 min, the fiber was nearly totally pyrolyzed and and kept fibrous carbonaceous although the specimen became too brittle to stand any load thereon.     

Preparation of zeolite-A/chitosan hybrid composites and their bioactivities and antimicrobial activities

Zeolite-A/chitosan hybrid composites with zeolite contents of 20–55 wt.% were prepared by in situ transformation of silica/chitosan mixtures in a sodium aluminate alkaline solution through impregnation–gelation–hydrothermal synthesis. The products were characterized by X-ray diffraction, diffuse reflectance infrared Fourier transform spectroscopy, scanning electron microscopy, thermogravimetric analysis, and mercury penetration porosimetry. Their in vitro bioactivities were examined using as-synthesized and Ca^2 +-exchanged hybrid composites in simulated body fluid (SBF) for hydroxyapatite (HAP) growth. Their antimicrobial activities for Escherichia coli (E. coli) in trypticase soy broth (TSB) were evaluated using Ag⁺-exchanged hybrid composites. The zeolite-A/chitosan hybrid composites could be prepared as various shapes, including cylinders, plates and thin films. They possessed macropores with pore sizes ranging from 100 to 300 μm and showed compressive mechanical strength as high as 3.2 MPa when the zeolite content was 35 wt.%. Fast growth on the Ca^2 +-exchanged hybrid composites was observed with the highest weight gain of 51.4% in 30 days. The 35 wt.% Ag⁺-exchanged hybrid composite showed the highest antimicrobial activity, which could reduce the 9 × 10⁶ CFU mL^? 1 E. coli concentration to zero within 4 h of incubation time with the Ag⁺-exchanged hybrid composite amount of 0.4 g L^? 1. The bioactivity and antimicrobial activity could be combined by ion-exchanging the composites first with Ca^2 + and then with Ag⁺. These zeolite-A/chitosan hybrid composites have potential applications on tissue engineering and antimicrobial food packaging.     

Highly mechanical strength and thermally conductive bismaleimide–triazine composites reinforced by Al2O3@polyimide hybrid fiber

Bismaleimide–triazine (BT) resins have received a great deal of attention in microelectronics due to its excellent thermal stability and good retention of mechanical properties. Thereafter, developing BT based composites with high mechanical strength, thermal conductivity and dielectric property simultaneously are highly desirable. In this study, one hybrid fiber of Al₂O₃ nanoparticle (200 nm) supported on polyimide fiber (Al₂O₃@PI) with core–shell structure was introduced into BT resin to prepare promising Al₂O₃@PI–BT composite. The results indicated that the resultant composites possessed high Young’s modulus of 4.06 GPa, low dielectric constant (3.38–3.50, 100 kHz) and dielectric loss (0.0102–0.0107, 100 kHz). The Al₂O₃@PI hybrid film was also conductive to improve thermal stability (T_d5% up to 371 °C), in-plane thermal conductivity (increased by 295% compared to that of the pure BT resin). Furthermore, the Al₂O₃@PI–BT composite were employed to fabricate a printed circuit substrate, on which a frequency “flasher” circuit and electrical components worked well.