Mechanical,thermal and morphological characterization of cellulose fiber-reinforced phenolic foams

In this work, the compressive mechanical properties, thermal stability and morphology of cellulose fiber-reinforced phenolic foams were studied. The cellulose fiber-reinforced phenolic foam showed the greatest compressive mechanical properties by incorporating 2 wt.% of the reinforcement. The compressive modulus and strength of 2 wt.% cellulose fiber-reinforced phenolic foam were increased by 21% and 18%, respectively, relative to the unreinforced material. The addition of the cellulose fibers to the phenolic foam slightly decreased the thermal stability of the material. The study on the morphology of the cellulose-reinforced phenolic foams via Scanning electron microscopy (SEM) indicated a strong bonding between the fibers and phenolic matrix. In addition, the incorporation of the cellulose fibers into the foam resulted in a decreased cell size and increased cell density of the material. The incorporation of 2 wt.% of cellulose fibers into the phenolic foam led to obtain the material with the best features.     

Semi-rigid biopolyurethane foams based on palm-oil polyol and reinforced with cellulose nanocrystals

In this study, water-blown biopolyurethane (BPU) foams based on palm oil were developed and cellulose nanocrystals (CNC) were incorporated to improve the mechanical properties of the foams. In addition, the foams were compared with petroleum polyurethane (PPU) foam. The foam properties and cellular morphology were characterized. The obtained results revealed that a low-density, semi-rigid BPU foam was prepared using a new formulation. CNC as an additive significantly improved the compressive strength from 54 to 117 kPa. Additionally, cyclic compression tests indicated that the addition of CNC increased the rigidity, leading to decreased deformation resilience. The dimensional stability of BPU foams was increased with increasing CNC concentration for both heating and freezing conditions.Therefore, the developed BPU nanocomposite foams are expected to have great potential as core material in composite sandwich panels as well as in other construction materials.     

Durability of GFRP nanocomposites subjected to hygrothermal ageing

This paper presents long term durability prediction of 0–5 wt.% nanoclay/vinylester/glass fibre nanocomposites based on their tensile strength retention in accelerated hygrothermal ageing using Arrhenius rate model. The specimens were exposed to 30 °C, 50 °C and 60 °C and 95% relative humidity for 75 days and tested for tensile strength retention as a function of duration of exposure. The predicted tensile strength retentions for one year of ageing of vinylester/glass at 30 °C, 50 °C and 60 °C using Arrhenius rate model were 59%, 48% and 43% respectively. The corresponding strength retentions predicted for 4 wt.% nanoclay/vinylester/glass were 81.1%, 77.9% and 76.4%. Strength retentions for ten years were predicted using the analytical model to assess their long-term performance.     

Synergistic effect of boron nitride flakes and tetrapod-shaped ZnO whiskers on the thermal conductivity of electrically insulating phenol formaldehyde composites

Tetrapod-shaped zinc oxide (T-ZnO) whiskers and boron nitride (BN) flakes were employed to improve the thermal conductivity of phenolic formaldehyde resin (PF). A striking synergistic effect on thermal conductivity of PF was achieved. The in-plane thermal conductivity of the PF composite is as high as 1.96 W m⁻¹ K⁻¹ with 30 wt.% BN and 30 wt.% T-ZnO, which is 6.8 times higher than that of neat PF, while its electrical insulation is maintained. With 30 wt.% BN and 30 wt.% T-ZnO, the flexural strength of the composite is 312.9% higher than that of neat PF, and 56.2% higher that of the PF composite with 60 wt.% BN. The elongation at break is also improved by 51.8% in comparison with that of the composite with 60 wt.% BN. Such a synergistic effect results from the bridging of T-ZnO whiskers between BN flakes facilitating the formation of effective thermal conductance network within PF matrix.     

Lignin particle- and wood flour-reinforced phenolic foams: Friability,thermal stability and effect of hygrothermal aging on mechanical properties and morphology

In the present work, the effect of lignin particles and wood flour weight fractions incorporated on friability and thermal stability of a phenolic foam was determined. In addition, the effect of hygrothermal aging on compressive mechanical properties and cell size of the materials was studied. The incorporation of lignin particles decreased friability of the phenolic foam; whereas, wood flour increased it. The influence of both reinforcements on thermal stability of the material was very low. Although the reduction in mechanical properties of reinforced foams was higher than for the unreinforced material after hygrothermal aging, modulus and strength of the reinforced foams were still superior to those of the unreinforced material. Hygrothermal aging did not influence cell size of the foams studied. The material which exhibits the best combination of features was 8.5 wt.% lignin particle-reinforced phenolic foam.     

Effect of different carbon nano-fillers on rheological properties and lap shear strength of epoxy adhesive joints

In this work, the rheological properties, thermal stability and the lap shear strength of epoxy adhesive joints reinforced with different carbon nano-fillers such as multi-walled carbon nanotubes (CNT), graphene nanoplatelets (GNP) and single-walled carbon nanohorns (CNH) have been studied. The nano-fillers were dispersed homogeneously using Brabender® Plasti-Corder®. The epoxy pre-polymer with and without the nano-fillers exhibited shear thinning behavior. The nano-filler epoxy mixtures exhibited a viscoplastic behavior which was analyzed using Casson’s model. Thermo-gravimetric analysis indicated an increase in the thermal stability of the epoxy with the addition of carbon nano-fillers. Carbon nano-fillers resulted in increased lap shear strength having high Weibull modulus. The joint strength increased by 53%, 49% and 46% with the addition of 1 wt.% CNT, 0.5 wt.% GNP and 0.5 wt.% CNH, respectively. The strength of the joints having high filler content (>1 wt.%) was limited by mixed mode type of failure.     

Effect of silica coating thickness on the thermal conductivity of polyurethane/SiO2 coated multiwalled carbon nanotube composites

Silica coated multiwalled carbon nanotubes (SiO₂@MWCNTs) with different coating thicknesses of ∼4 nm, 30–50 nm, and 70–90 nm were synthesized by a sol–gel method and compounded with polyurethane (PU). The effects of SiO₂@MWCNTs on the electrical properties and thermal conductivity of the resulting PU/SiO₂@MWCNT composites were investigated. The SiO₂ coating maintained the high electrical resistivity of pure PU. Meanwhile, incorporating 0.5, 0.75 and 1.0 wt% SiO₂@MWCNT (70–90 nm) into PU, produced thermal conductivity values of 0.287, 0.289 and 0.310 W/mK, respectively, representing increases of 62.1%, 63.3% and 75.1%. The thermal conductivity of PU/SiO₂@MWCNT composites was also increased by increasing the thickness of the SiO₂ coating.     

Functionalizing graphene decorated with phosphorus-nitrogen containing dendrimer for high-performance polymer nanocomposites

In this paper, we demonstrate a novel strategy for fabricating advanced polymer composites based on functionalized graphene oxide decorated with phosphorus-nitrogen-containing dendrimers (PND-GO). Both X-ray diffraction and transmission electron microscopy results show that reduced PND-GO uniformly disperses within polymer matrix and is exfoliated in polyurethane (PU) via in situ polymerization. Cone calorimetry results show that incorporating 2 wt% reduced PND-GO into PU decreases the peak heat release rate by 53% and prolongs the time to ignition by 28 s as compared with the PU bulk. Besides, the tensile strength and Young’s modulus are remarkably enhanced by about 2 times and 5 times, respectively.     

Enhanced conductivity behavior of polydimethylsiloxane (PDMS) hybrid composites containing exfoliated graphite nanoplatelets and carbon nanotubes

Polydimethylsiloxane (PDMS) hybrid composites consisting of exfoliated graphite nanoplatelets (xGnPs) and multiwalled carbon nanotubes functionalized with hydroxyl groups (MWCNTs-OH) were fabricated, and the effects of the xGnP/MWCNT-OH ratio on the thermal, electrical, and mechanical properties of polydimethylsiloxane (PDMS) hybrid composites were investigated. With the total filler content fixed at 4 wt%, a hybrid composite consisting of 75% × GnP/25% MWCNT-OH showed the highest thermal conductivity (0.392 W/m K) and electrical conductivity (1.24 × 10⁻³ S/m), which significantly exceeded the values shown by either of the respective single filler composites. The increased thermal and electrical conductivity found when both fillers are used in combination is attributed to the synergistic effect between the fillers that forms an interconnected hybrid network. In contrast, the various different combinations of the fillers only showed a modest effect on the mechanical behavior, thermal stability, and thermal expansion of the PDMS composite.     

Cross-linked nanocomposite hydrogels based on cellulose nanocrystals and PVA: Mechanical properties and creep recovery

Cellulose nanocrystal (CNC) reinforced poly(vinyl alcohol) (PVA) hydrogels with a water content of ∼92% were successfully prepared with glutaraldehyde (GA) as a cross-linker. The effects of the CNC content on the thermal stability, swelling ratio and mechanical and viscoelastic properties of the cross-linked hydrogels were investigated. The compressive strength at 60% strain for the hydrogels with 1 wt% CNCs increased by 303%, from 17.5 kPa to 53 kPa. The creep results showed that the addition of CNCs decreased the creep elasticity due to molecular chain restriction. The almost complete strain recovery (∼97%) after fixed load removal for 15 min was observed from the hydrogels with CNCs, compared with 92% strain recovery of the neat cross-linked PVA hydrogels. The incorporation of CNCs did not affect the swelling ratio and thermal stability of the hydrogels. These results suggest the cross-linked CNC-PVA hydrogels have potential for use in biomedical and tissue engineering applications.     

High thermal conductivity of flexible polymer composites due to synergistic effect of multilayer graphene flakes and graphene foam

Research on flexible thermal interface materials (TIMs) has shown that the interconnected network of graphene foam (GF) offers effective paths of heat transportation. In this work, a variant amount of multilayer graphene flakes (MGFs) was added into 0.2 vol% GF/polydimethylsiloxane (PDMS) composite. A remarkable synergistic effect between MGF and GF in improving thermal conductivity of polymer composites is achieved. With 2.7 vol% MGFs, the thermal conductivity of MGF/GF/PDMS composite reaches 1.08 W m⁻¹ K⁻¹, which is 80%, 184% and 440% higher than that of 2.7 vol% MGF/PDMS, GF/PDMS composites and pure PDMS, respectively. The MGF/GF/PDMS composite also shows superior thermal stability. The addition of MGFs and GF decreases slightly the elongation at break, but observably increases the Young’s modulus and tensile strength of composites compared with pure PDMS. The good performance of MGF/GF/PDMS composite makes it a good TIM for possible application in thermal management of electronics.     

Chemical functionalization of graphene oxide for improving mechanical and thermal properties of polyurethane composites

Graphene oxide (GO) was chemically functionalized to prepare polyurethane (PU) composites with improved mechanical and thermal properties. In order to achieve a well exfoliated and stable GO suspension in an organic solvent (dimethylformamide, DMF), 4, 4′-methylenebis(phenyl isocyanate) and polycaprolactone diol, which were the two monomers for synthesizing PU, were selectively used to functionalize GO. The obtained functionalized GO (FGO) could form homogeneous dispersions in DMF solvent and the PU matrix, as well as provide a good compatibility with the PU matrix. The most efficient improvement of mechanical properties was achieved when 0.4 wt.% FGO was added into the PU matrix, showing increases in the tensile stress, elongation at break and toughness by 34.2%, 27.6%, and 64.5%, respectively, compared with those of PU. Regarding the thermal stability, PU filled with 1 wt.% FGO showed the largest extent of improvement with T_2% and T_50% (the temperatures at which 2% and 50% weight-loss happened) 16 °C and 21 °C higher than those of PU, respectively. The significant improvement in both mechanical properties and thermal stability of FGO/PU composites should be attributed to the homogeneous dispersion of FGO in the PU matrix and strong interfacial interaction between them.     

Heat treated wood–nylon 6 composites

Heat treatment is a relatively benign modification method that is growing as an industrial process to improve hygroscopicity, dimensional stability and biological resistance of lignocellulosic fillers. There also has been increased interest in the use of lignocellulosic fillers in numerous automotive applications. This study investigated the influence of untreated and heat treated wood fillers on the mechanical and rheological properties of wood filled nylon 6 composites for possible under-the-hood applications in the automobile industry where conditions are too severe for commodity plastics to withstand. In this study, exposure of wood to high temperatures (212 °C for 8 h) improved the thermal stability and crystallinity of wood. Heat treated pine and maple filled nylon 6 composites (at 20 wt.% loading) had higher tensile strengths among all formulations and increased tensile strength by 109% and 106% compared to neat nylon 6, respectively. Flexural modulus of elasticity (FMOE) of the neat nylon 6 was 2.34 GPa. The FMOE increased by 101% and 82% with the addition of 30 wt.% heat treated pine and 20 wt.% heat treated maple, where it reached maximum values of 4.71 GPa and 4.27 GPa, respectively. The rheological properties of the composites correlated with the crystallinity of wood fillers after the heat treatment. Wood fillers with high crystallinity after heat treatment contributed to a higher storage modulus, complex viscosity and steady shear viscosity and low loss factor in the composites. This result suggests that heat treatment substantially affects the mechanical and rheological properties of wood filled nylon 6 composites. The mechanical properties and thermogravimetric analysis indicated that the heat treated wood did not show significant thermal degradation under 250 °C, suggesting that the wood-filled nylon composites could be especially relevant in thermally challenging areas such as the manufacture of under-the-hood automobile components.     

Aramid fibers reinforced silica aerogel composites with low thermal conductivity and improved mechanical performance

Aramid fibers reinforced silica aerogel composites (AF/aerogels) for thermal insulation were prepared successfully under ambient pressure drying. The microstructure showed that the aramid fibers were inlaid in the aerogel matrix, acting as the supporting skeletons, to strengthen the aerogel matrix. FTIR revealed AF/aerogels was physical combination between aramid fibers and aerogel matrix without chemical bonds. The as prepared AF/aerogels possessed extremely low thermal conductivity of 0.0227 ± 0.0007 W m⁻¹ K⁻¹ with the fiber content ranging from 1.5% to 6.6%. Due to the softness, low density and remarkable mechanical strength of aramid fibers and the layered structure of the fiber distribution, the AF/aerogels presented nice elasticity and flexibility. TG–DSC indicated the thermal stability reaching approximately 290 °C, can meet the general usage conditions, which was mainly depended on the pure silica aerogels. From mentioned above, AF/aerogels present huge application prospects in heat preservation field, especially in piping insulation.     

Size-scale effects of silica on bis-GMA/TEGDMA based nanohybrid dental restorative composites

The present study focuses on the effect of size-scale combination of silica on the mechanical and dynamic mechanical properties of acrylate based (50% Bis-GMA and 50% TEGDMA by weight) composites with an aim to overcome the conventional problem of high-volume fraction filling of acrylate based composites, typically used in restorative dentistry. Two classes of light-cured composites based on the size-scale combination of silica (7 nm + 2 μm; 14 nm + 2 μm) as the filler were prepared. FTIR spectroscopy revealed functionality and interactions whereas morphological investigations concerning the state of distribution and dispersion of nano- and micro-silica has been carried out by SEM–EDX Si-dot mapping. The dynamic mechanical properties, compressive, flexural and diametral tensile strengths were characterized. Micromechanical analysis of viscoelastic storage moduli following Kerner composite model has revealed an enhancement in the reinforcement efficiency of the nanohybrid composites based on the filler size-scale combination of 14 nm + 2 μm with 10 wt.% nanofiller loading. The compressive strength of the micro-filled composite (with 2 μm silica only) was found to remain comparable to that of the nanohybrid with 5 wt.% of 7 nm silica and 10 wt.% of 14 nm silica filled composites. Diametral tensile strength has been observed to be influenced by the size-scale combination and extent of nanofiller loading. The effective volume fractions in the composites validating the experimentally determined DTS were calculated following Nicolais–Narkis model. Our study demonstrates the conceptual feasibility of exploring the optimization of size-scale combinations of filler for enhancement in reinforcement efficiency by manipulating the volume fraction of filler induced immobilized polymer chains by resorting to the principle of micromechanics.     

Improved mechanical properties of an epoxy glass–fiber composite reinforced with surface organomodified nanoclays

An organomodified surface nanoclay reinforced epoxy glass-fiber composite is evaluated for properties of mechanical strength, stiffness, ductility and fatigue life, and compared with the pristine or epoxy glass-fiber composite material not reinforced with nanoclays. The results from monotonic tensile tests of the nanoclay reinforced composite material at 60 °C in air showed an average 11.7% improvement in the ultimate tensile strength, 10.6% improvement in tensile modulus, and 10.5% improvement in tensile ductility vs. these mechanical properties obtained for the pristine material. From tension–tension fatigue tests at a stress-ratio = +0.9 and at 60 °C in air, the nanoclay reinforced composite had a 7.9% greater fatigue strength and a fatigue life over a decade longer or 1000% greater than the pristine composite when extrapolated to 10⁹ cycles or a simulated 10-year cyclic life. Electron microscopy and Raman spectroscopy of the fracture and failure modes of the test specimens were used to support the results and conclusions. This nanocomposite could be used as a new and improved material for repair or rehabilitation of external surface wall corrosion or physical damage on piping and vessels found in petrochemical process plants and facilities to extend their operational life.     

Solvent infusion processing of all-cellulose composite laminates using an aqueous NaOH/urea solvent system

All-cellulose composites are high performing green materials and solvent infusion processing makes their upscaled manufacturing possible. This study explored the use of aqueous 7 wt.% NaOH/12 wt.% urea solution as cost effective and environmentally friendly cellulose solvent for solvent infusion processing. A short dissolution time of 5 min led to all-cellulose composite laminates with a tensile strength of 114 ± 1.9 MPa and a Young’s modulus of 7.8 ± 0.5 GPa. A decrease of tensile strength and Young’s modulus with increasing dissolution time from 5 to 60 min was linked to changes in composite microstructure and fine structure of the reinforcing rayon fibres. It was shown that aqueous NaOH/urea solution is a promising alternative solvent, as it offers the advantages of shorter processing times and reduced solvent costs by 97%, while resulting in 25% stronger laminates, when compared to using ionic liquids.     

Study on thermal properties of graphene foam/graphene sheets filled polymer composites

The polymer composites composed of graphene foam (GF), graphene sheets (GSs) and pliable polydimethylsiloxane (PDMS) were fabricated and their thermal properties were investigated. Due to the unique interconnected structure of GF, the thermal conductivity of GF/PDMS composite reaches 0.56 W m⁻¹ K⁻¹, which is about 300% that of pure PDMS, and 20% higher than that of GS/PDMS composite with the same graphene loading of 0.7 wt%. Its coefficient of thermal expansion is (80–137) × 10⁻⁶/K within 25–150 °C, much lower than those of GS/PDMS composite and pure PDMS. In addition, it also shows superior thermal and dimensional stability. All above results demonstrate that the GF/PDMS composite is a good candidate for thermal interface materials, which could be applied in the thermal management of electronic devices, etc.     

Effects of temperature and clay content on water absorption characteristics of modified MMT clay/cyclic olefin copolymer nanocomposite films: Permeability,dynamic mechanical properties and the encapsulated organic device performance

In the present study, amino-silane modified layered organosilicates were used to reinforce cyclic olefin copolymer to enhance the thermal, mechanical and moisture impermeable barrier properties. The optimum clay loading (4%) in the nanocomposite increases the thermal stability of the film while further loading decreases film stability. Water absorption behavior at 62 °C was carried out and compared with the behavior at room temperature and 48 °C. The stiffness of the matrix increases with clay content and the recorded strain to failure for the composite films was lower than the neat film. Dynamic mechanical analysis show higher storage modulus and low loss modulus for 2.5–4 wt% clay loading. Calcium degradation test and device encapsulation also show the evidence of optimum clay loading of 4 wt% for improved low water vapor transmission rates compared to other nanocomposite films.     

Investigation of the effect of nanoclay and processing parameters on the tensile strength and hardness of injection molded Acrylonitrile Butadiene Styrene–organoclay nanocomposites

Polymer–clay nanocomposites have attracted considerable interest over recent years due to their dramatic improved mechanical properties. In the present study, compatibility of Acrylonitrile Butadiene Styrene (ABS) and organically modified montmorillonite nanoclay (Cloisite 30B) and composition capability of them are investigated. Polymethylmethacrylate (PMMA) in varying amount (0, 2, and 4 wt%) is used as the compatibilizer. In order to produce nanocomposite parts, the material is first compounded using a twin-screw extruder and then injected into a mold. The effect of the nanoclay percentage and processing parameters on the tensile strength and hardness of nanocomposite parts is also explored using Taguchi Design of Experiments method. Nanoclay content (in three levels: 0, 2 and 4 wt%), melt temperature (in three levels: 190, 200 and 210 °C), holding pressure (in three levels: 80, 105 and 130 MPa) and holding pressure time (in three levels: 1, 2.5 and 4 s) are considered as the variable parameters. Moreover, distribution of nanoclay layers is analyzed using Wide Angle X-ray Diffraction (XRD) test. XRD results displayed that with the presence of PMMA, nanoclay in ABS matrix is compounded in more exfoliated and less intercalated dispersion mode. Adding PMMA also leads to a remarkable increase in the fluidity of the melt during injection molding process. Results also illustrated that nanocomposites with medium loading level (i.e. 2%) of nanoclay have the highest tensile strength, while the highest hardness number belongs to nanocomposites with 4 wt% nanoclay. Obtained results also indicated that injection temperature has the most important effect on tensile strength and hardness of ABS–clay nanocomposites.