Woven hybrid biocomposites: Dynamic mechanical and thermal properties

The dynamic mechanical and thermal analysis of oil palm empty fruit bunch (EFB)/woven jute fibre (J_w) reinforced epoxy hybrid composites were carried out. The storage modulus (E′) was found to decrease with temperature in all cases, and hybrid composites had showed better values of E′ at glass transition temperature (T_g) compared to EFB and epoxy. Loss modulus showed shifts in the T_g of the polymer matrix with the addition of fibre as reinforcing phase, which indicate that fibre plays an important role in case of T_g. The Tan δ peak height was minimum for jute composites and maximum for epoxy matrix. Complex modulus variations and phase behaviour of the hybrid composites was studied by Cole-Cole analysis. Thermal analysis result indicates an increase in thermal stability of EFB composite with the incorporation of woven jute fibres. Hybridization of EFB composite with J_w fibres enhanced the dynamic mechanical and thermal properties.     

Morphology, dynamic mechanical and thermal studies on poly(styrene-co-acrylonitrile) modified epoxy resin/glass fibre composites

Poly(styrene-co-acrylonitrile) (SAN) was used to modify diglycidyl ether of bisphenol-A (DGEBA) type epoxy resin cured with diamino diphenyl sulfone (DDS) and the modified epoxy resin was used as the matrix for fibre reinforced composites (FRPs) in order to get improved mechanical and thermal properties. E-glass fibre was used as the fibre reinforcement. The morphology, dynamic mechanical and thermal characteristics of the systems were analyzed. Morphological analysis revealed heterogeneous dispersed morphology. There was good adhesion between the matrix polymer and the glass fibre. The dynamic moduli, mechanical loss and damping behaviour as a function of temperature of the systems were studied using dynamic mechanical analysis (DMA). DMA studies showed that DDS cured epoxy resin/SAN/glass fibre composite systems have two T_gs corresponding to epoxy rich and SAN rich phases. The effect of thermoplastic modification and fibre loading on the dynamic mechanical properties of the composites were also analyzed. Thermogravimetric analysis (TGA) revealed the superior thermal stability of composite system.     

Study on the mechanical properties and thermal properties of jute and banana fiber reinforced epoxy hybrid composites

The aim of the present study is to investigate and compare the mechanical and thermal properties of raw jute and banana fiber reinforced epoxy hybrid composites. To improve the mechanical properties, jute fiber was hybridized with banana fiber. The jute and banana fibers were prepared with various weight ratios (100/0, 75/25, 50/50, 25/75 and 0/100) and then incorporated into the epoxy matrix by moulding technique to form composites. The tensile, flexural, impact, thermal and water absorption tests were carried out using hybrid composite samples. This study shows that addition of banana fiber in jute/epoxy composites of up to 50% by weight results in increasing the mechanical and thermal properties and decreasing the moisture absorption property. Morphological analysis was carried out to observe fracture behavior and fiber pull-out of the samples using scanning electron microscope.     

Comparison of the mechanical and physical properties of a carbon fibre epoxy composite manufactured by resin transfer moulding using conventional and microwave heating

Microwave processing holds great potential for improving current composite manufacturing techniques, substantially reducing cure cycle times, energy requirements and operational costs. In this paper, microwave heating was incorporated into the resin transfer moulding technique. Through the use of microwave heating, a 50% cure cycle time reduction was achieved. The mechanical and physical properties of the produced carbon fibre/epoxy composites were compared to those manufactured by conventional resin transfer moulding. Mechanical testing showed similar values of flexural moduli and flexural strength for the two types of composites after normalisation of the corresponding data to a common fibre volume fraction. A 9% increase of the interlaminar shear strength (ILSS) was observed for the microwave cured composites. This enhancement in ILSS is attributed to a lowering of resin viscosity in the initial stage of the curing process, which was also confirmed via scanning electron microscopy by means of improved fibre wetting and less fibre pull-out. Furthermore, both types of composites yielded minimal void content (<2%). Dynamic mechanical thermal analysis revealed comparable glass transition temperatures for composites produced by both methods. A 15 °C shift in the position of the β-transition peak was observed between thermally and microwave cured composites, suggesting an alteration in the cross-linking path followed.     

Viscoelastic properties of multi-walled carbon nanotube/epoxy composites using two different curing cycles

Along with carbon nanotubes (CNT) morphology, impurity, and functionalization, polymer curing cycle is another important factor in determining the mechanical properties of the CNT/polymer composite samples. This work investigates the effect of two different curing cycles on mechanical and thermo-mechanical properties of the nanotube in the composite in order to optimize the curing condition in term of time and temperature. Nanocomposite samples were prepared by mixing multi-wall carbon nanotubes with epoxy resin using sonication method. The mechanical and viscoelastic properties of the resulting composite samples were evaluated by performing tensile and dynamic mechanical thermal analyses (DMTA) test. The results indicate that the mechanical and viscoelastic properties of pure epoxy and composite samples have been affected by the condition curing process. Concerning viscoelastic modeling, the COLE–COLE diagram has been plotted by the result of DMTA tests. These results show a good agreement between the Perez model and the viscoelastic behavior of the composite.     

Thermo-physical properties of epoxy nanocomposites reinforced with amino-functionalized multi-walled carbon nanotubes

The modification of multi-walled carbon nanotubes (MWNTs) with amine groups was investigated by FTIR, Raman spectroscopy and XPS after such steps as carboxylation, acylation and amidation. Nanotube-reinforced epoxy polymer composites were prepared by mixing amino-functionalized MWNTs with epoxy resin and curing agent. DSC, TGA, SEM and flexural test were used to investigate the thermal and mechanical properties of the composites. The results showed that amino-functionalized MWNTs could enhance the interfacial adhesion between the nanotubes and the matrix, thus greatly improve the thermal and mechanical properties of the resin epoxy bulk material.     

酚化酶解木质素-环氧树脂/环氧树脂复合材料的合成及性能

以酶解木质素(EHL)为原料,采用苯酚-硫酸法对其进行酚化改性,所得酚化木质素(PL)在碱性条件下,与环氧氯丙烷(ECH)合成木质素-环氧树脂(L-EP),利用FT-IR对产物进行表征。探讨单因素反应条件对酚化工艺的影响。结果表明:反应时间3.0h、反应温度95℃、2mol/L H_2SO_4用量为4mL/g时,木质素的酚化效果最佳,其酚羟基含量达到4.632mmol/g,较EHL提高42%。研究了不同L-EP添加量对L-EP/环氧E-51复合材料力学性能和热性能的影响。结果显示:L-EP的添加量为5%时,L-EP/环氧E-51复合材料的拉伸强度最好,较纯E-51提高26%;随着L-EP添加量的增加,L-EP/环氧E-51复合材料的热稳定性增强。采用非等温法分析环氧E-51和L-EP/环氧E-51复合材料的固化动力学,结果证明:L-EP对复合材料固化有一定的促进作用。     

Mechanical properties of epoxy composites with high contents of nanodiamond

Mechanical properties and thermal conductivity of composites made of nanodiamond with epoxy polymer binder have been studied in a wide range of nanodiamond concentrations (0-25 vol.%). In contrast to composites with a low content of nanodiamond, where only small to moderate improvements in mechanical properties were reported before, the composites with 25 vol.% nanodiamond showed an unprecedented increase in Young’s modulus (up to 470%) and hardness (up to 300%) as compared to neat epoxy. A significant increase in scratch resistance and thermal conductivity of the composites were observed as well. The improved thermal conductivity of the composites with high contents of nanodiamond is explained by direct contacts between single diamond nanoparticles forming an interconnected network held together by a polymer binder.     

Non-stoichiometric curing effect on fracture toughness of nanosilica particulate-reinforced epoxy composites

Non-stoichiometric curing effects on the fracture toughness behaviors of nanosilica particulate-reinforced epoxy composites were experimentally investigated in this study by comparing them with bending strengths to take into consideration the effect of interaction between nanoparticles and network structures in matrix resins. The matrixes were prepared by curing them with an excess mixture of diglycidyl ether of bisphenol A-type epoxy resin as the curing agent for the stoichiometric condition. The volume fractions of the silica particles with a median diameter of 240 nm were constantly 0.2 for all composites. The neat epoxy resins and the composites were cured non-stoichiometrically to change the crosslinking densities of the neat epoxy resins and the matrix resins of the composites within 2740–490 mol/m³. The fracture toughnesses and bending strengths of the composites and the neat epoxy resins strongly depended on the crosslinking densities in the resins. Although the fracture toughness decreased monotonously from that of the stoichiometrically cured resins as the crosslinking density decreased, the fracture toughnesses of composites were largest at a slightly lower crosslinking density of approximately 2490 mol/m³ from the stoichiometric condition of 2740 mol/m³. The fracture toughness and the bending strength were improved for crosslinking densities higher than 2000 mol/m³ by adding particles. At crosslinking density lower than 2000 mol/m³, the particles worked against the mechanical properties as defects in matrix resins.     

Mechanical properties of epoxy composites reinforced with a low volume fraction of nanosilica fillers

In this paper we focus on the preparation and mechanical properties of the nanosilica-reinforced, epoxy resin Epikote 828LVEL. Epoxy composites containing two sizes of spherical silica nanoparticles, 130 nm and 30 nm, were prepared at a fixed volume fraction (V_P = 0.5%). To prevent agglomeration, the silica fillers were initially pre-treated with diglycidyl ether of bisphenol A (BADGE). Due to the low content of silica fillers, their inclusion in the matrix was confirmed by the increased roughness of a fracture surface compared to the smooth surface of the neat epoxy. Raman spectroscopy was employed to obtain additional information about the crack-propagation path. The mechanical properties, characterized by a three-point bending test, revealed a 10–20% increase in the composite's modulus of elasticity with 30-nm and 130-nm silica-filler inclusions. Elongation at break, on the other hand, decreased for 5–10% in both composites compared to neat epoxy, suggesting brittle fracture behavior in silica/epoxy composites. The fracture toughness results showed a 25–30% improved toughening for both composites compared to the pure epoxy. The composite's resistance to failure in terms of the impact energy was, however, strongly dependent on the size of the silica: we observed a 30% increase for the 130-nm, and a 60% increase for the 30-nm, silica/epoxy composites, compared to the pure epoxy.     

Mechanical properties of epoxy composites filled with silane-functionalized graphene oxide

In this work, the effects of as-produced GO and silane functionalized GO (silane-f-GO) loading and silane functionalization on the mechanical properties of epoxy composites are investigated and compared. Such silane functionalization containing epoxy ended-groups is found to effectively improve the compatibility between the silane-f-GO and the epoxy matrix. Increased storage modulus, glass transition temperature, thermal stability, tensile and flexural properties and fracture toughness of epoxy composites filled with the silane-f-GO sheets are observed compared with those of the neat epoxy and GO/epoxy composites. These findings confirm the improved dispersion and interfacial interaction in the composites arising from covalent bonds between the silane-f-GO and the epoxy matrix. Moreover, several possible fracture mechanisms, i.e. crack pinning/deflection, crack bridging, and matrix plastic deformation initiated by the debonding/delamination of GO sheets, were identified and evaluated.     

The reinforcing effect of graphene nanosheets on the cryogenic mechanical properties of epoxy resins

The reinforcing effect of graphene in enhancing the cryogenic tensile and impact properties of epoxy composites is examined at a weight fraction of 0.05–0.50%. The micro-structure and cryogenic mechanical properties of the graphene/epoxy composites are investigated using scanning electron microscopy, transmission electron microscopy, small-angle X-ray scattering and mechanical testing techniques. The results show that the graphene dispersion in the epoxy matrix is good at low contents while its aggregation takes place and becomes severer as its content increases. And the cryogenic tensile and impact strength at liquid nitrogen temperature (77 K) of the composites are effectively improved by the graphene addition at proper contents. The cryogenic Young’s modulus increases almost linearly with increasing the graphene content. Moreover, the results for the mechanical properties at room temperature (298 K) of the graphene/epoxy composites are also presented for the purpose of comparison.     

Synergistic effects of PEK-C/VGCNF composite nanofibres on a trifunctional epoxy resin

Polyetherketone cardo (PEK-C) nanofibres containing vapour-grown carbon nanofibres (VGCNFs) were electrospun, and used for toughening and reinforcing a triglycidyl amino phenol (TGAP) epoxy resin. The addition of PEK-C/VGCNF nanofibres to the epoxy resin led to the distribution of VGCNFs primarily within the phase separated PEK-C-rich domains. Synergistic effects of thermoplastic PEK-C and VGCNFs on the mechanical properties, phase morphologies and thermal stability of the resultant epoxy matrix composites were observed when the PEK-C/CNF nanofibres were blended at a low content into the epoxy resin. Strong and tough multifunctional nanocomposites were prepared with the addition of 5 wt.% PEK-C/CNF nanofibres to the epoxy matrix.     

Mechanical and thermal characterization of epoxy composites reinforced with random and quasi-unidirectional untreated Phormium tenax leaf fibers

The present work investigates tensile and flexural behavior of untreated New Zealand flax (Phormium tenax) fiber reinforced epoxy composites. Two series of laminates were produced using the same reinforcement content (20 wt%), arranged either as short fibers or quasi-unidirectional ones. Composites reinforced using quasi-unidirectional fibers showed higher modulus and strength both in tensile and flexural loading, when compared to neat epoxy resin. Short fiber composites, although still superior to epoxy resin both for tensile and flexural moduli, proved inferior in strength, especially as concerns tensile strength. These results have been supported by scanning electron microscopy (SEM), which allowed characterizing fiber–matrix interface, and by acoustic emission (AE) analysis, which enabled investigating failure mechanisms. In addition, thermal behavior of both untreated phormium fibers and composites has been studied by thermogravimetric analysis (TGA), revealing the thermal stability of composites to be higher than for phormium fibers and epoxy matrix alone.     

环氧树脂及其复合材料微波固化研究进展

在介绍微波固化技术的原理及其优点的基础上,综述了环氧树脂及其复合材料的微波固化研究进展,重点讨论了微波固化对环氧树脂及其复合材料固化体系的固化速率、固化产物力学性能和热性能的影响,介绍了颗粒增强环氧树脂和纤维增强环氧树脂两种适合微波固化的复合材料系及工业应用关键技术问题,并对环氧树脂及其复合材料微波固化的应用前景进行了展望。     

Introducing cellulose nanocrystals in sheet molding compounds (SMC)

The mechanical properties of short glass fiber/epoxy composites containing cellulose nanocrystals (CNC) made using sheet molding compound (SMC) manufacturing method as well as the rheological and thermomechanical properties of the CNC-epoxy composites were investigated as a function of the CNC content. CNC up to 1.4 wt% were dispersed in the epoxy to produce the resin for SMC production. The addition of CNC in the resin increased its viscosity and slightly reduced the heat of reaction during the polymerization without altering the curing time and temperature and the effective pot life of the resin. The incorporation of 0.9 wt% CNC in the SMC composite resulted in increases in elastic modulus and tensile strength by ∼25% and ∼30% and in flexural modulus and strength by ∼44% and ∼33% respectively. Concentrations of CNC up to 0.9 wt% in the SMC composite did not alter the impact energy.     

Improvement of the Compressive Strength of Carbon Fiber/Epoxy Composites via Microwave Curing

Microwave processing was used to cure the carbon fiber/epoxy composites and designed for improving the compressive strength of the materials. By controlling the power of microwave heating, vacuum bagged laminates were fabricated under one atmosphere pressure without arcing. The physical and mechanical properties of composites produced through vacuum bagging using microwave and thermal curing were compared and the multistep(2-step or 3-step) microwave curing process for improved compressive properties was established. The results indicated that microwave cured samples had somewhat differentiated molecular structure and showed slightly higher glass transition temperature. The 2-step process was found to be more conducive to the enhancement of the compressive strength than the 3-step process. A 39% cure cycle time reduction and a 22% compressive strength increment were achieved for the composites manufactured with microwave radiation. The improvement in specific compressive strength was attributed to better interfacial bonding between resin matrix and the fibers, which was also demonstrated via scanning electron microscopy analysis.     

Thermal conductive and electrical properties of polyurethane/hyperbranched poly(urea-urethane)-grafted multi-walled carbon nanotube composites

Hyperbranched poly(urea-urethane)-grafted multi-walled carbon nanotubes (HPU-MWCNTs) were incorporated in a polyurethane (PU) matrix based on poly(ethylene oxide-tetrahydrofuran) and aliphatic polyisocyanate resin as curing agent. The 9–12 nm thick HPU shell formed on the MWCNTs improved the dispersion of MWCNTs and enhanced the interfacial adhesion between the PU matrix and MWCNTs, leading to improvements in storage modulus and T_g of the composites and enhancement of the thermal stability of PU. Thus, composites with 0.5–1 wt% MWCNTs increased the thermal conductivity by about 60–70% when compared to, and retained the high electrical resistivity of, neat PU.     

Preparation and characterization of water-borne epoxy shape memory composites containing silica

Shape memory silica/epoxy composites were successfully prepared by hydrolysis of tetraethoxysilane (TEOS) within the epoxy matrix via latex, freeze-drying, and hot-press molding method. The silane coupling agent 3-triethoxysilylpropylamine (KH550) was introduced to improve the interfacial properties between the in-situ generated silica particle and epoxy matrix. The morphology structure and the effect of the content of the in-situ formed silica on the mechanical and shape memory properties of the silica/epoxy composites were studied. The experimental results indicated that the silica particles were homogenously dispersed and well incorporated into the epoxy matrix. Significant improvements were achieved in the mechanical property of the organic–inorganic hybrid materials. The silica/epoxy composites exhibited high shape recovery and fixity ratio approximately 100% even after 10 thermo-mechanical cycles.     

Viscoelastic and mechanical properties of multi walled carbon nanotube/epoxy composites with different nanotube content

The viscoelastic and mechanical properties of composites multi walled carbon nanotube (MWNT)/epoxy at different weight fractions (0.1, 0.5, 1 and 2 wt.%) were evaluated by performing tensile and dynamic-mechanical thermal analysis (DMTA) tests. The MWNT/epoxy composite were fabricated by sonication and a cast molding process. The results showed that addition of nanotubes to epoxy had significant effect on the viscoelastic and mechanical properties. However, the use of 0.5 wt.% increased the viscoelastic properties more significantly. Concerning viscoelastic modeling, the COLE–COLE diagram has been plotted by the results of DMTA test. These results show a good agreement between the Perez model and the viscoelastic behavior of the composite.