Lithium aluminosilicate reinforced with carbon nanofiber and alumina for controlled-thermal-expansion materials

Materials with a very low or tailored thermal expansion have many applications ranging from cookware to the aerospace industry. Among others, lithium aluminosilicates (LAS) are the most studied family with low and negative thermal expansion coefficients. However, LAS materials are electrical insulators and have poor mechanical properties. Nanocomposites using LAS as a matrix are promising in many applications where special properties are achieved by the addition of one or two more phases. The main scope of this work is to study the sinterability of carbon nanofiber (CNFs)/LAS and CNFs/alumina/LAS nanocomposites, and to adjust the ratio among components for obtaining a near-zero or tailored thermal expansion. Spark plasma sintering of nanocomposites, consisting of commercial CNFs and alumina powders and an ad hoc synthesized β-eucryptite phase, is proposed as a solution to improving mechanical and electrical properties compared with the LAS ceramics obtained under the same conditions. X-ray diffraction results on phase compositions and microstructure are discussed together with dilatometry data obtained in a wide temperature range (−150 to 450 °C). The use of a ceramic LAS phase makes it possible to design a nanocomposite with a very low or tailored thermal expansion coefficient and exceptional electrical and mechanical properties.     

Surface coating on carbon nanofibers with alumina precursor by different synthesis routes

Alumina-reinforced carbon nanofiber nanocomposites were prepared using different routes; powders mixture, colloidal route and sol-gel process followed by spark plasma sintering (SPS). CNFs/xAl₂O₃ (x = 10-50 vol.%) were prepared through nanopowders mixing in a high-energy attrition milling. The main limitations in the preparation of this kind of nanocomposites are related to the difficulty in obtaining materials with a homogeneous distribution of both phases and the different chemical nature of CNFs and Al₂O₃, which causes poor interaction between them. A surface coating of CNFs by wet chemical routes with an alumina precursor is proposed as a very effective way to improve the interaction between CNFs and Al₂O₃. An improvement of 50% in fracture strength was found for similar nanocomposite compositions when the surface coating was used. The improved mechanical properties of these nanocomposites are caused by stronger interaction between the CNFs and Al₂O₃.     

Fe-based metallic glass particles reinforced Al-7075 matrix composites prepared by spark plasma sintering

Metallic glass (MG) reinforced aluminum matrix composites (AMCs) have attracted the interest of many researchers in the past few years. In this study, Fe₅₀Cr₂₅Mo₉B₁₃C₃ metallic glass (FMG) particles reinforced 7075 aluminum matrix (Al-7075) composites were prepared by spark plasma sintering (SPS) technique. The microstructure of the composites showed good interface bonding between the FMG particles and the matrix. The micro-hardness of the composite with 30 vol% FMG particles reached 160.63 HV, which was increased by 30% compared with that of Al-7075 (119.3 HV). The ultimate compression strength (UCS) of the composite was also improved significantly from 596 MPa for Al-7075 matrix to 749 MPa for the composite reinforced with 30 vol% FMG particles, and the compression strain of the composite reached 22%. These results indicate that the mechanical properties of the composites can be enhanced by adding high volume fraction FMG particles. The enhancement of the strength is resulted from multiple strengthening mechanisms, and the main contributions come from the thermal mismatch and grain refinement.     

High temperature electrical and thermal properties of the bulk carbon nanotube prepared by SPS

Bulk multi-walled carbon nanotube was prepared by spark plasma sintering at 1700 °C under a pressure of 50 MPa in vacuum. The density of the bulk sample reaches 72% of the theoretical density of the carbon nanotube, 2 g/cm³. The high temperature thermal conductivity and electrical conductivity of the bulk material were measured in the directions perpendicular and parallel to the pressure direction. Both the thermal conductivity and electrical conductivity show apparent anisotropy. The thermoelectric power has close values in the two different directions and takes positive values in the whole measured temperature range (360–840 K).     

Fabrication and mechanical properties of carbon short fiber reinforced barium aluminosilicate glass–ceramic matrix composites

Dense BaSi₂Al₂O₈ (BAS) and Ba_0.75Sr_0.25Si₂Al₂O₈ (BSAS) glass–ceramic matrix composites reinforced with carbon short fibers (C_sf) were fabricated by hot pressing technique. The microstructure, mechanical properties and fracture behavior of the composites were investigated by X-ray diffraction, scanning and transmission electron microscopies, and three-point bend tests. The carbon fibers had a good chemical compatibility with the glass–ceramic matrices and can effectively reinforce the BAS (or BSAS) glass–ceramic because of associated toughening mechanisms such as crack deflection, fiber bridging and pullout effects. Doping of BAS with 25 mol% SrSi₂Al₂O₈ (SAS) can accelerate the hexacelsian to celsian transformation and result in the formation of pure monoclinic celsian in C_sf/BSAS composites, which can avoid the undesirable reversible hexacelsian to orthorhombic transformation at 300 °C and reduce the thermal expansion mismatch between the fiber and matrix.     

Reinforcing polyamide 1212 nanocomposites with aligned carbon nanofibers

In this study, the mechanical properties and structure orientation of pure polyamide 1212 (PA1212) were compared with those of PA1212–carbon nanofibers (CNFs) nanocomposites. The tensile strength of the composite containing 0.3 wt.% modified CNFs was improved from 328 MPa (pure PA1212) to 373 MPa after drawing. The reinforcing effect was investigated in terms of crystallization behavior, crystal morphology, alignment of CNFs, and crystal orientation degree. Spherulites developed into oriented crystals after drawing, and the CNFs aligned along the drawing direction. The heterogeneous nucleation effect of the aligned CNFs improved the crystal orientation degree, which produced the reinforcing effect. The oriented fibril structures with rigid nanofibers acting as nuclei reinforced the entire oriented crystals in the composites.     

Pristine and amino functionalized carbon nanotubes reinforced glass fiber epoxy composites

Multi-phase composites have been studied by incorporating carbon nanotubes (CNTs) as a secondary reinforcement in an epoxy matrix which was then reinforced with glass fiber mat. Different types of CNTs e.g. amino functionalized carbon nanotubes (ACNT) and pristine carbon nanotubes (PCNT) were homogeneously dispersed in the epoxy matrix and two-ply laminates were fabricated using vacuum-assisted resin infusion molding technique. The issues related to CNT dispersion and interfacial bonding and its affect on the mechanical properties have been studied. An important finding of this study is that PCNT scores over ACNT in composites prepared under certain conditions. This is a very significant finding since PCNT is available at a much lower cost than ACNT.     

Investigation of carbon nanotube reinforced aluminum matrix composite materials

We have increased the tensile strength without compromising the elongation of aluminum (Al)–carbon nanotube (CNT) composite by a combination of spark plasma sintering followed by hot-extrusion processes. From the microstructural viewpoint, the average thickness of the boundary layer with relatively low CNT incorporation has been observed by optical, field-emission scanning electron, and high-resolution transmission electron microscopies. Significantly, the Al–CNT composite showed no decrease in elongation despite highly enhanced tensile strength compared to that of pure Al. We believe that the presence of CNTs in the boundary layer affects the mechanical properties, which leads to well-aligned CNTs in the extrusion direction as well as effective stress transfer between the Al matrix and the CNTs due to the generation of aluminum carbide.     

Mechanical property characterization of carbon nanofiber/epoxy nanocomposites reinforced by GMA-grafted UHMWPE fibers

Carbon nanofibers (CNFs) dispersed epoxy resin was reinforced with unidirectional glycidyl methacrylate (GMA) grafted ultra-high molecular weight polyethylene (UHMWPE) fibers. Tensile tests were performed on unfilled, and CNF filled epoxy to identify the effect of adding CNFs on the mechanical properties of epoxy. The highest improvement in strength was obtained with 1 wt% of CNF. Tensile and flexural properties improvements in three-component nanocomposites were confirmed by obtained results. The combined use of CNFs and GMA-grafted UHMWPE fibers leads to a significant synergy in the mechanical properties of nanocomposites. The mechanisms of such synergism were analyzed by fracture studies using scanning electron microscopy.     

Microstructure and mechanical properties of in situ TiB reinforced titanium matrix composites based on Ti–FeMo–B prepared by spark plasma sintering

The in situ synthesized TiB reinforced titanium matrix composites have been prepared by spark plasma sintering at 800–1200 °C under 20 MPa for 5 min. The effects of sintering temperature and reinforcement volume fraction on flexural strength, Young’s modulus and fracture toughness of the composites are investigated. The titanium matrix consists of -Ti and β-Ti phases, and the volume fraction of β-Ti increases with increasing sintering temperatures. The in situ synthesized TiB reinforcements are distributed randomly and uniformly in matrix. The transverse section of TiB has a hexagonal shape aligned along [0 1 0] direction, and the crystallographic planes of the TiB needles are always of the type . The 10 vol% TiB reinforced composite sintered at 1000 °C exhibits excellent mechanical properties. The flexural strength, Young’s modulus and fracture toughness of this composite are 1560 MPa, 137 GPa and 8.64 MPa · m^1/2, respectively.     

Mechanical characterization of hierarchical carbon fiber/nanofiber composite laminates

Susceptibility to matrix driven failure is one of the major weaknesses of continuous-fiber composites. In this study, helical-ribbon carbon nanofibers (CNF) were dispersed in the matrix phase of a continuous carbon fiber-reinforced composite. Along with an unreinforced control, the resulting hierarchical composites were tested to failure in several modes of quasi-static testing designed to assess matrix-dominated mechanical properties and fracture characteristics. Results indicated CNF addition offered simultaneous increases in tensile stiffness, strength and toughness while also enhancing both compressive and flexural strengths. Short-beam strength testing resulted in no apparent improvement while the fracture energy required for the onset of mode I interlaminar delamination was enhanced by 35%. Extrinsic toughening mechanisms, e.g., intralaminar fiber bridging and trans-ply cracking, significantly affected steady-state crack propagation values. Scanning electron microscopy of delaminated fracture surfaces revealed improved primary fiber–matrix adhesion and indications of CNF-induced matrix toughening.     

Interconnected multi-walled carbon nanotubes reinforced polymer-matrix composites

A modified method for interconnecting multi-walled carbon nanotubes (MWCNTs) was put forward. And interconnected MWCNTs by reaction of acyl chloride and amino groups were obtained. Scanning electron microscopy shows that hetero-junctions of MWCNTs with different morphologies were formed. Then specimens of pristine MWCNTs, chemically functionalized MWCNTs and interconnected MWCNTs reinforced epoxy resin composites were fabricated by cast moulding. Tensile properties and fracture surfaces of the specimens were investigated. The results show that, compared with pristine MWCNTs and chemically functionalized MWCNTs, the chemically interconnected MWCNTs improved the fracture strain and therefore the toughness of the composites significantly.     

Review of the mechanical properties of carbon nanofiber/polymer composites

In this paper, the mechanical properties of vapor grown carbon nanofiber (VGCNF)/polymer composites are reviewed. The paper starts with the structural and intrinsic mechanical properties of VGCNFs. Then the major factors (filler dispersion and distribution, filler aspect ratio, adhesion and interface between filler and polymer matrix) affecting the mechanical properties of VGCNF/polymer composites are presented. After that, VGCNF/polymer composite mechanical properties are discussed in terms of nanofibers dispersion and alignment, adhesion between the nanofiber and polymer matrix, and other factors. The influence of processing methods and processing conditions on the properties of VGCNF/polymer composite is also considered. At the end, the possible future challenges for VGCNF and VGCNF/polymer composites are highlighted.     

Stress-dependence and time-dependence of the post-fatigue tensile behavior of carbon fiber reinforced SiC matrix composites

The major objective of this paper is to phenomenally report the stress-dependence and time-dependence of fatigue damage to C/SiC composites, and to tentatively discuss the effects of the fatigue stress levels and the fatigue cycles on the post-fatigue tensile behavior. Results show that compared with the virgin strength of the as-received C/SiC specimens, the tensile strengths of the as-fatigued specimens after 86,400 cycles were increased by 8.47% at the stresses of 90 ± 30 MPa, 23.47% at 120 ± 40 MPa, and 9.8% at 160 ± 53 MPa. As cycles continued, however, the post-fatigue strength of the composites gradually decreased after the peak of 23.47%, at which the optimal strength enhancement was obtained because the mean fatigue stress of 120 MPa was the closest to thermal residual stress (TRS), and caused TRS relieve largely during the fatigue. Most interestingly, there was a general inflexion appeared on the post-fatigue tensile stress-strain curves, which was just equal to the historic maximum fatigue stress acted upon the as-fatigued specimens. Below this inflexion stress the tensile curves revealed the apparent linear behavior with little AE response, and above that nonlinearity with new damage immediately emitted highly increase rate of AE activities. This ‘stress memory’ characteristic was strongly relevant to damaged microstructures of the as-fatigued composites in the form of the coating/matrix cracks, interface debonding/wear, and fiber breaking, which resulted undoubtedly in reduction of modulus but in proper increase of strength via TRS relief.     

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.     

放电等离子烧结高合金工具钢的组织与性能

本文研究了放电等离子烧结（SPS）参数对HGSF01高合金工具钢致密度、硬度的影响规律,以及烧结态HGSF01高合金工具的显微组织、抗弯强度和摩擦磨损性能。结果表明：材料的致密度随烧结温度的升高和保温时间的延长呈上升趋势,而硬度则是先升高后降低;经SPS得到的材料晶粒细小,晶粒尺寸约为5μm,碳化物颗粒细小、均匀、弥散分布在基体上;烧结态材料的抗弯强度比电渣重熔态材料提高了一倍,耐磨性比电渣重熔态材料略有提高。     

A novel high-entropy alloy with multi-scale precipitates and excellent mechanical properties fabricated by spark plasma sintering

Body-centered-cubic (BCC) high entropy alloys (HEAs) usually exhibit high strength but poor ductility. To overcome such strength-ductility trade-off, a novel (FeCr)₄₅(AlNi)₅₀Co₅ HEA was presented in this paper, which was designed and fabricated with mechanical alloying (MA) followed by spark plasma sintering (SPS), and has a heterogeneous microstructure with multi-scale precipitates. Electron microscopy characterization revealed that the sizes of the precipitates range from nano (<300 nm), sub-micron (300～800 nm) to micron (>1 μm). The bulk HEA exhibits excellent mechanical properties, of which the compressive yield strength, fracture strength, and plasticity at room temperature can reach 1508 MPa, 3106 MPa and 30.4 %, respectively, which are much higher than that of most HEAs prepared by Powder Metallurgy reported in the literatures, suggesting that the HEA developed is highly promising for engineering applications. The excellent mechanical properties of the bulk HEA can be attributed to that the multi-scale precipitates are fully coherent with the matrix, which could reduce the misfit strain at the interface, and relieve the stress concentration during deformation.     

Highly dispersed graphene oxide electrodeposited carbon fiber reinforced cement-based materials with enhanced mechanical properties

Mechanical behavior of carbon fiber (CF) reinforced cement-based materials greatly depends on the dispersion of CF and interfacial properties between the CF and cement matrix. In this study, graphene oxide (GO) was utilized to modify the surface properties of CF, including the roughness, wettability and chemical reactivity, and the graphene oxide/carbon fiber (GO/CF) hybrid fibers were fabricated by a newly designed electrophoretic depositing method. The scanning electron microscopy and contact angle measurement results indicated that GO/CF hybrid fibers not only had a rougher surface which was expected to improve the physical friction when CF was pulled out from cement matrix, but also had a higher wettability surface that made it easier to contact with cement hydrates as nucleation sites. In addition, GO/CF hybrid fibers were capable of high chemical reactivity due to the introduction of GO with many functional groups, which ensured them more likely to interact with cement hydrates due to the hydrogen bonding at interface and therefore benefited to strengthen the bonding between the CF and cement matrix. In terms of mechanical behavior, three-point bending test showed that compared with the CF reinforced cement paste, flexural strength of the GO/CF hybrid fibers reinforced cement paste was enhanced by 14.58%, and could be further improved by 10.53% when the GO/CF hybrid fibers were pre-dispersed in the GO solution and then mixed with cement powders. The larger electrostatic repulsion and steric stabilization led to the better dispersion of GO/CF hybrid fibers in GO solution, which were responsible for the further mechanical enhancement of cement paste. In conclusion, the research outcomes provided a novel way for utilizing GO as both of dispersant and surface modifier to improve the dispersion of CF in cement and strengthen its bonding with cement hydrates, consequently achieving a significant enhancement in the mechanical properties of cement paste.     

Free-standing functional graphene reinforced carbon films with excellent mechanical properties and superhydrophobic characteristic

In this work, we reported a simple method to fabricate novel free-standing stiff carbon-based composite films with excellent mechanical properties and superhydrophobic behaviors. The free-standing stiff carbon composite films based on reduced graphene oxide/glassy carbon (rGO/GC) were prepared by the combination of in-situ polymerization and carbonization process. The obtained composite films exhibited excellent mechanical properties by the addition of rGO nanosheets. It was found that incorporating 0.5 wt.% of rGO sheets in GC precursors resulted in enhancements of 99% in strength (202.6 MPa) and 184% in modulus (33.8 GPa), respectively. More interestingly, carbon nanoarrays were uniformly grown on the surface of composite films by the incorporation of rGO sheets. Superhydrophobic surfaces of carbon films were subsequently formed through functionalizing carbon nanoarrays with Trichloro(1H, 1H, 2H, 2H-perfluorodecyl)silane. Contact angle (CA) analysis suggested that superhydrophobic surfaces with a CA as high as 155° could be formed through optimizing the fabrication process.     

Microstructure and mechanical properties of spark plasma sintered austenitic ODS steel

In this work, austenitic oxide dispersion strengthened (AODS) steel of composition Fe–16Cr–16Ni–1.5 W–0.21Ti–0.3Y₂O₃ (wt. %) was fabricated using two–stage ball milling followed by consolidation through spark plasma sintering (SPS). In the first–stage, mechanical alloying (MA) of ferritic powder and nano sized Y₂O₃ was carried out. This was followed by the addition of Ni in second–stage milling. SPS of the milled powder was carried out at 900, 950, 1000 and 1050 °C to explore the role of SPS temperature on density, microstructure as well as mechanical properties of the consolidated samples. A relative density of ～ 99% was obtained for samples sintered at 950 and 1000 °C. The as–sintered samples were subsequently solution annealed at 1075 °C for 2 h and water quenched. X–ray diffraction studies confirmed the presence of austenite in the consolidated and solution annealed samples. Electron back scatter diffraction analysis of solution annealed samples sintered at all the temperatures revealed a bimodal microstructure. The average grain size of 1.07 ± 0.72 µm was obtained for solution annealed samples sintered at 1000 °C. Yield strength and elongation of the same was measured as 851 MPa and 18%, respectively at room temperature. These values are the best combination of strength to elongation achieved on AODS alloys processed using MA and SPS, which makes this AODS steel much promising for high temperature applications.