Hybrid silane-treated glass fabric/epoxy composites: tensile properties by micromechanical approach

The effect of interface modification on the interfacial adhesion and tensile properties of glass fabric/epoxy composites was evaluated in two directions of 0° and +45°. Herein, the glass fabric surface was modified by colloidal nanosilica particles and by a new blend of silane-coupling agents including both reactive and non-reactive silanes. Composite samples with high strength and toughness were obtained. A simultaneous improvement of tensile strength and toughness was observed for an epoxy composite reinforced with a hybrid-sized glass fabric including silane mixture and nanosilica. In fact, the incorporation of colloidal silica into the hybrid sizing dramatically modified the fiber surface texture and created mechanical interlocking between the glass fabric and resin. The results were analyzed by the rule of mixtures (ROM), Halpin–Tsai (H–T), and Chamis equations. It was found that the ROM equations provided approximate upper bound values for all investigated composite samples. In the samples containing nanosilica, the shear and elastic moduli values calculated by the Chamis and ROM equations showed good agreement with those obtained from experiments. However, in other samples, the values calculated by the H–T equation showed a better agreement with the experimental data. The analysis of fracture surfaces indicated that both silane and nanosilica particles had influence on the mode of failures at the interface.     

碳纤维/聚苯并(噁)嗪复合材料的界面与力学性能的关系研究

本文采用含不同上胶剂的碳纤维与苯并(噁)嗪树脂复合,制备碳纤维/聚苯并(噁)嗪单向复合材料,研究了碳纤维表面上胶剂对于复合材料的层间剪切强度(ILSS)、弯曲性能、断口形貌及动态机械性能的影响.结果表明,含有环氧树脂上胶剂的碳纤维/苯并(噁)嗪树脂基复合材料(EPCF/PBZ)的ILSS和弯曲性能优于含非环氧类树脂上胶剂的碳纤维/苯并(噁)嗪树脂基复合材料(VECF/PBZ)和不含上胶剂的碳纤维/苯并(噁)嗪树脂基复合材料(USCF/PBZ).环氧树脂上胶剂改善了纤维与苯并(噁)嗪树脂的粘结性能,使复合材料的内耗峰峰高降低,能量损耗减小.电镜照片同样验证了这一结果.     

Effect of macromolecular coupling agent on the property of PP/GF composites

Silane‐grafted polypropylene manufactured by a reactive grafting process was used as the coupling agent in polypropylene/glass‐fiber composites to improve the interaction of the interfacial regions. Polypropylene reinforced with 30% by weight of short glass fibers was injection‐molded and the mechanical behaviors were investigated. The results indicate that the mechanical properties (tensile strength, tensile modulus, flexural strength, flexural modulus, and Izod impact strength) of the composite increased remarkably as compared with the noncoupled glass fiber/polypropylene. SEM of the fracture surfaces of the coupled composites shows a good adhesion at the fiber/matrix interface: The fibers are coated with matrix polymer, and a matrix transition region exists near the fibers. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1537–1542, 1999     

Microstructural,mechanical, and thermal characteristics of recycled cellulose fiber‐halloysite‐epoxy hybrid nanocomposites

Epoxy hybrid‐nanocomposites reinforced with recycled cellulose fibers (RCF) and halloysite nanotubes (HNTs) have been fabricated and investigated. The dispersion of HNTs was studied by synchrotron radiation diffraction (SRD) and transmission electron microscopy (TEM). The influences of RCF/HNTs dispersion on the mechanical properties and thermal properties of these composites have been characterized in terms of flexural strength, flexural modulus, fracture toughness, impact toughness, impact strength, and thermogravimetric analysis. The fracture surface morphology and toughness mechanisms were investigated by SEM. Results indicated that mechanical properties increased because of the addition of HNTs into the epoxy matrix. Flexural strength, flexural modulus, fracture toughness, and impact toughness increased by 20.8, 72.8, 56.5, and 25.0%, respectively, at 1 wt% HNTs load. The presence of RCF dramatically enhanced flexural strength, fracture toughness, impact strength, and impact toughness of the composites by 160%, 350%, 444%, and 263%, respectively. However, adding HNTs to RCF/epoxy showed only slight enhancements in flexural strength and fracture toughness. The inclusion of 5 wt% HNTs into RCF/epoxy ecocomposites increased the impact toughness by 27.6%. The presence of either HNTs or RCF accelerated the thermal degradation of neat epoxy. However, at high temperature, samples reinforced with RCF and HNTs displayed better thermal stability with increased char residue than neat resin. POLYM. COMPOS. 2012. © 2012 Society of Plastics Engineers     

原位聚合连续纤维增强聚甲基丙烯酸甲酯复合材料的界面及性能研究

通过选用含不同官能团的硅烷偶联剂3-甲基丙烯酰氧丙基三甲氧基硅烷(MPS)、γ-氨丙基三甲氧基硅烷(APS)和γ-氯丙基三甲氧基硅烷(CPS)处理玻璃纤维,然后通过原位聚合的方法制造了连续纤维增强的聚甲基丙烯酸甲酯(PMMA)复合材料。研究结果表明,经过这三种偶联剂处理的玻璃纤维与基体树脂在界面分别形成了化学键、范德华力和氢键。红外、动态力学分析和扫描电镜研究表明,复合材料的界面粘接强度顺序为:MPS>CPS>APS。MPS处理的复合材料具有最高的弯曲强度,而CPS处理的复合材料具有最佳的冲击韧性和断裂伸长率。     

Mechanical properties of hybrid structural composites reinforced with nanosilica

Epoxy‐based hybrid structural composites reinforced with 14 nm spherical silica particles were investigated for mechanical properties as a function of nanosilica loading fractions. Composites were fabricated using continuous glass or carbon fiber of unidirectional architecture and nanosilica dispersed epoxy, through resin film infusion process. Uniform dispersion of nanoparticles in resin matrix was ensured by an optimized ultrasound‐assisted process. Although resin viscosity marginally reduces in the presence of nanosilica enabling a better control in composite manufacturing process, glass transition temperature of epoxy remained unaffected at low weight fractions. Compressive strength of hybrid glass or carbon fiber/epoxy composites showed more than 30–35% increase with nanosilica at a concentration as low as 0.2 wt%. Tensile and compressive properties of hybrid composites in transverse direction to the reinforcement remained unaffected. POLYM. COMPOS. 37:1216–1222, 2016. © 2014 Society of Plastics Engineers     

Mechanical performance of woven carbon fabric reinforced pCBT composites with nanosilica particles

The effect of nanosilica content (0, 0.5, and 2 wt%) on mechanical performance of carbon fabric woven cloth reinforced polymerized poly(butylene terephthalate) resin composites (CF/pCBT) is investigated. The catalyst and nanosilica particles are added on the prepreg surface, and hot‐press processing is adopted in order to manufacture CF/pCBT composites. The experimental results reveal that nanosilica could enhance the mechanical performance of CF/pCBT composites. After adding nanosilica in the composites, elastic modulus enhances 23.96%, and Mode‐II fracture toughness increases 380.43%. Scanning electron microscope observation shows that dispersity of nanoparticles in composites plays an important role on the overall mechanical performance of the obtained composites. Furthermore, failure mechanism has been analyzed according to the damage morphology. POLYM. COMPOS., 38:2528–2535, 2017. © 2015 Society of Plastics Engineers     

环氧树脂/短切碳纤维复合材料性能研究

制备出了短切碳纤维增强TDE-85环氧树脂复合材料,研究了碳纤维的含量对复合材料力学性能和耐热性能的影响。结果表明,碳纤维的加入有利于复合材料力学性能和耐热性能的提高,并在碳纤维含量为0.25%时,复合材料的拉伸强度、冲击韧性、弯曲强度和弯曲模量达到最大,分别提高了29.33%、25.31%、30.28%和68.93%。此外,对复合材料的弯曲断裂面进行了微观形貌分析,结果表明一定量的碳纤维可以较好地分散在树脂基体中,同时,碳纤维原丝和树脂基体的界面结合比较弱,主要依赖于两相之间的物理嵌合。     

Performance improvement of rubber-modified polybenzoxazine

Polybenzoxazine as a noble phenolic resin was modified with amine-terminated butadiene acrylronitrile rubber (ATBN) and with carboxyl-terminated butadiene acrylronitrile rubber (CTBN) in order to improve its mechanical properties. The fracture toughness, flexural modulus, and flexural strength of rubber-modified polybenzoxazine were measured to investigate the effect of rubber modification. In fracture toughness, ATBN is more effective than CTBN. ATBN-modified polybenzoxazine showed better distribution of rubber particles in matrix phase than did CTBN-modified polybenzoxazine. The cure rates in these systems were monitored by differential scanning calorimetry to investigate the effect of cure rate on rubber size. The change of glass transition temperatures of rubber-modified polybenzoxazine was measured with a dynamic mechanical thermal analyzer to explain the variation of mechanical properties. In addition, the relationship between mechanical properties and the morphology of rubber-modified polybenzoxazines was also undertaken. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 67: 1–10, 1998     

Effects of copper amine treatment on mechanical properties of PVC/wood‐flour composites

Copper amine–treated wood flour was added to PVC [poly(vinyl chloride)] matrix in order to manufacture PVC/wood‐flour composites. Effects of copper treatments on the mechanical properties of PVC‐wood composites were evaluated. Unnotched impact strength, flexural strength, and flexural toughness of the composites were significantly improved by the wood‐flour copper treatment. The optimum copper concentration range was 0.2 to 0.6 wt% of wood flour. Fractured surfaces were examined by using scanning electron microscopy (SEM) combined with energy‐dispersive spectroscopy (EDS). PVC/wood interfacial debonding was the main fracture mode of untreated wood‐flour composites, whereas wood‐particle pullout and breakage dominating the fractured surfaces of copper‐treated wood‐flour composites. On the fractured surfaces, more PVC could be found on the exposed copper‐treated wood particles than on untreated wood, a result suggesting improved PVC‐wood interfacial adhesion after copper treatments. J. Vinyl Addit. Technol. 10:70–78, 2004. © 2004 Society of Plastics Engineers.     

Effect of organosilane coupling agents on microstructure and properties of nanosilica/epoxy composites

Three types of silane coupling agents, γ‐aminopropyltriethoxysilane, γ‐glycidoxypropyltrimethoxysilane, and γ‐methacryloxypropyltrimethoxysilane, were used as modifiers to modify the surface of the nanosilica, respectively, and the nanocomposites of the epoxy resin filled with nano‐sized silica modified by three silane coupling agents were prepared by physical blending. The properties of the modified silica nanoparticles were characterized by Fourier transform infrared spectrum and particle‐size analyzer. The microstructure, mechanical behavior, and heat resistant properties of the nanocomposites were investigated by transmission electron microscopy, scanning electron microscopy, thermo gravimetric analyses, differential thermal gravity, differential scanning calorimetry, and flexural tests. The results showed that these modifiers are combined to the surfaces of nanosilica by the covalent bonds, and they change the surface properties of nanosilica. The different structures of coupling agents have different effects on the dispersibility and stability of modified particles in the epoxy matrix. In comparison, the silica nanoparticles modified by γ‐glycidoxypropyltrimethoxysilane exhibit a good dispersivity. The nanocomposites with 4 wt% weight fraction nanosilica modified by γ‐glycidoxypropyltrimethoxysilane have higher thermal decomposing temperature and glass transition temperature than those of the other two composites with the same nanosilica contents, and they are raised by 43.8 and 8°C relative to the unmodified composites, respectively. The modified silica nanoparticles have good reinforcing and toughening effect on the epoxy matrix. The ultimate flexural strengths of the composites with 4 wt% nanoparticles modified by γ‐aminopropyltriethoxysilane, γ‐glycidoxypropyltrimethoxysilane, and γ‐methacryloxypropyltrimethoxysilane are increased by 10, 30, and 8% relative to the unmodified composites, respectively. The flexural fracture surfaces of modified composites present ductile fracture features. POLYM. COMPOS. 2012. © 2012 Society of Plastics Engineers     

Surface modification of hollow glass microsphere with different coupling agents for potential applications in phenolic syntactic foams

Modified hollow glass microsphere (HGM) particles have been prepared by surface treatment. Coupling agents such as γ‐aminopropyltriethoxysilane (APTES), di(dioctylpyrophosphato) ethylene titanate (NDZ‐311), and glutaraldehyde (GA) were used as modifiers to improve the hydrophobicity of HGM. Compared with pristine HGM, the modified HGM, especially the particles coupled with APTES‐GA, show better properties on flexural strength, fracture toughness, and dynamic mechanical properties of phenolic syntactic foams. It is revealed that the coupling agent coating layer grafted onto the surface of HGM reduces the polarity of particles, avoiding agglomeration of HGM in phenolic matrix and exhibiting good interfacial interaction between HGM and phenolic matrix. The remarkable improvement of interfacial adhesion between APTES‐GA modified HGM and phenolic matrix is mainly due to the covalent linkage with phenolic resin while the physical entanglement of molecular chains dominates the linkage between other modified HGM and phenolic matrix. APTES‐GA treatment is a more appropriate surface modification method for inorganic particle reinforced phenolic matrix composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44415.     

短玻纤增强聚丙烯的研究进展

综述了近年来有关短玻纤增强聚丙烯复合材料的力学性能、变形机理和断裂韧性等方面的研究工作。短玻纤取向后的复合材料注射样的力学性能是各向异性的 ,复合材料在取向方向上具有更高的拉伸强度。玻纤与树脂基体间界面结合力的强弱对材料的力学性能同样起着至关重要的作用。良好的界面结合力保证了应力有效地从基体向玻纤传递 ,从而提高了复合材料的强度。由于短玻纤的分布既不均匀又不规则 ,在受到负荷时的变形过程很复杂 ,包括玻纤 -基体的界面脱黏、脱黏后的摩擦、基体的塑性变形、玻纤的塑性变形、玻纤断裂、基体断裂和玻纤抽出等     

PET interleaving veils for improved fracture toughness of glass fibre/low‐styrene‐emission unsaturated polyester resin composites

The use of interleaved polyethylene terephthalate (PET) veils to increase the interlaminar fracture toughness of glass fiber‐reinforced, low‐styrene emission, unsaturated polyester resin composites, was investigated. PET, being chemically similar to the unsaturated polyester resin, was expected to exhibit good wetting and strong interaction with the matrix. Composite laminates were manufactured by hand lay‐up, with the veil content varying up to 7%. The effects of PET veils on the interlaminar shear strength, flexural strength, flexural modulus, glass transition temperature, damping parameters, and Mode‐I interlaminar fracture toughness of the composite were studied. The veils were found to enhance most of these properties, with only minor negative effects on flexural stiffness and T_g. The PET/resin bonding did indeed prove to be strong, but the enhancement of fracture toughness was not as much as expected, because of the weaker glass/resin interface providing an alternative crack propagation path. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42877.     

PA66/RTMB/GF复合材料的结构与力学性能研究

采用玻璃纤维(GF)、反应性增韧母料(RTMB)与PA66热机械反应性共混制备出了PA66/RTMB/GF复合材料.用IR、SEM、力学性能测定等方法研究了PA66/RTMB/GF复合材料的化学结构、断面形态及力学性能.结果表明:PA66/RTMB/GF中RTMB、GF和PA66间形成了化学键连接,GF和PA66间呈柔性界面结合;PA66/RTMB/GF质量比为60/10/30的复合材料的拉伸屈服应力、弯曲弹性模量、悬臂梁缺口冲击强度分别提高到原料PA66的1.73倍、2.72倍、3.86倍.     

Highly filled thermoplastic composites. II: Effects of particle size distribution on some properties

The effect of irregularly shaped glass particle size and size distribution on the packing density and flexural mechanical properties of highly-filled composites with a rubbery thermoplastic matrix was studied. Increasing the particle's median size and size distribution width significantly increases the packing density of the composites. Compression molding causes the glass particles to fracture at a decreasing level with an increasing distribution width. Particle median size, rather than size distribution, affects the mechanical properties; The flexural modulus and strength increase and the ultimate deflection in flexure decreases with a decreasing median size. A “glass network” is formed in the compression molded composites because of the mechanical interlocking of particles. The nature of this continuous glass phase predominates the composites mechanical behavior. The particle's size and shape determine the nature of the glass network and, thus, have a dominating effect on the mechanical properties. The latter are significantly affected by the particle's surface properties. A specific silane treatment of the glass particles acts to reduce the particle/particle friction, resulting in a higher packing density. The treatment also acts as a cohesive liquid to increase the strength of the glass network, and to increase the particle/polymer adhesion, increasing the composites' strength and ductility.     

Effect of Coupling Agent Concentration,Fiber Content,and Size on Mechanical Properties of Wood/HDPE Composites

In this study, the influence of coupling agent concentration (0 and 3 wt%), wood fiber content (50, 60, 70, and 80 wt%), and size (40–60, 80–100, and 160–180 mesh) on the mechanical properties of wood/high-density-polyethylene (HDPE) composites (WPCs) was investigated. WPC samples were prepared with poplar wood-flour, HDPE, and polyethylene maleic anhydride copolymer (MAPE) as coupling agent. It was found that the tensile properties and the flexural properties of the composites were improved by the addition of 3 wt% MAPE, and the improved interfacial adhesion was well confirmed by SEM micrographs. It was also observed that the best mechanical properties of wood/HDPE composites can be reached with larger particle size in the range studied, while too-small particle size was adverse for the mechanical properties of wood/HDPE composites. Moreover, the tensile modulus, tensile strength, and flexural strength of WPCs decreased with the increase in fiber content from 50 to 80 wt%; the flexural modulus of WPCs increased with the increase in fiber content from 50 to 70 wt% and then decreased as the fiber content reached 80 wt%. The variances in property performance are helpful for the end-user to choose an appropriate coupling agent (MAPE) concentration, wood fiber content, and particle size based on performance needs and cost considerations.     

Mechanical Properties of Benzoylated Oil Palm Empty Fruit Bunch Short Fiber Reinforced Poly(vinyl chloride) Composites

The influence of untreated and benzoylated oil palm empty fruit bunch (OPEFB) short fiber loading on the mechanical properties of the poly(vinyl chloride) (PVC) composite was studied. Benzoylated OPEFB was produced by mixing OPEFB with NaOH solution and agitating vigorously with benzoyl chloride. The PVC resin, various additives, and OPEFB were first dry blended using a laboratory mixer before being milled into sheets on a two-roll mill at 165°C and then hot pressed into composite samples at 180°C. The tensile and impact strength of untreated and benzoylated OPEFB composites decreased whereas the tensile modulus increased with increasing fiber loading from 0 to 40 phr. However, the benzoylated OPEFB was able to improve the tensile properties and impact strength of composites when compared to the untreated fiber. The enhancement of mechanical properties showed that the treatment improved the OPEFB fiber-PVC matrix interfacial adhesion. The improvement of adhesion was clarified by SEM micrographs, the increase of water resistance, and the reduction of glass transition temperature of the composites.     

Dendritic polyamidoamine-grafted halloysite nanotubes for fabricating toughened epoxy composites

Well-dispersed epoxy resin/halloysite nanotubes composites were prepared by functionalization of the HNTs surfaces using polyamidoamine generation-3 (HNTs-G3.0). A series of modified halloysite nanotubes with different generations of dendritic polyamidoamine (PAMAM) were prepared via a divergent synthetic process by repeating the Michael addition of methyl acrylate to superficial amino groups and the amidation of the resulting esters with ethylenediamine. The products were then characterized by means of FTIR, XPS, XRD and TGA. The results showed that PAMAM polymers are successfully grafted on the surface of HNTs and the grafting percentage of HNTs grafted with polyamidoamine generation-3 (HNTs-G3.0) is 27.21 %. The grafted PAMAM has no effect on the crystalline structure of HNTs. The morphology, interfacial interaction and mechanical properties of epoxy composites were investigated and correlated with the surface functionalization of HNTs. The observations of scanning electronic microscopy and transmission electron microscopy images showed that HNTs-G3.0 exhibited better dispersion than the p-HNTs. The interfacial interaction of the epoxy composites was studied by FTIR and DMA. It was found that dendritic polyamidoamine graft can effectively improve the interfacial interaction of the epoxy composites. With the improvement in particle dispersion and interfacial interaction through polyamidoamine generation-3 grafting, an increase of impact strength and fracture toughness was achieved, accompanied by enhancements of flexural strength and modulus. In particular, the impact strength and fracture toughness (K _IC) of composites with polyamidoamine generation-3 grafted HNTs were about 160 and 20 % higher than the values of functionalization halloysite nanotube system.     

Effects of hygrothermal aging on the thermal–mechanical properties of vinylester resin and its pultruded carbon fiber composites

Hygrothermal aging was carried out on vinyl ester (VE) resin cast and its pultruded carbon fiber reinforced composite (CF/VE) by immersing them in distilled water at 65 and 95°C. Hygrothermal aging effects on the samples were studied in terms of thermal–mechanical properties, as well as moisture absorption behavior, interfacial adhesion, and transverse mechanical properties. Moisture absorption behaviors of the VE casts and the CF/VE composites were characterized as Fickian behavior. Dynamic mechanical thermal analysis (DMTA) tests showed that the tan δ peak temperatures of the VE casts and CF/VE composites decreased with immersion time at 65 and 95°C. Moreover, there existed a splitting in the tan δ peaks at 95°C, which was reversible and could be recovered by dehydration. Three‐point flexural test indicated that flexural strengths of both the VE casts and the composites decreased by hygrothermal aging with a trend related to their moisture absorption behaviors, while flexural modulus of the composites was less affected. The ILSS of the CF/VE composites was also depressed by deterioration in interfacial adhesion, which was proved by the interfacial adhesion parameters, A and α. POLYM. COMPOS., 2009. © 2009 Society of Plastics Engineers