Toughened carbon fiber fabric‐reinforced pCBT composites

Toughened carbon fiber‐fabric reinforced polymerized cyclic butylene terephthalate (pCBT) composites were obtained by chemical modification of cyclic butylene terephthalate (CBT) with small amounts of epoxy resin and isocyanates as chain extenders. Homogeneous CBT/epoxy and CBT/isocyanate blends were prepared by melt blending the components in a lab‐scale batch mixer at low temperatures and high shear rate. Melt blending was stopped before the ring‐opening polymerization of CBT could start. The modified CBT was the starting material for carbon fiber fabric‐reinforced pCBT composites (fiber content at about 65 wt%) which were prepared by ring‐opening polymerization during compression molding using a simple powder prepreg method. Interlaminar shear strength, flexural strength, and failure strain of the chemically modified composites increased up to 60% with respect to unmodified pCBT composites. Nevertheless, the flexural moduli slightly decreased due to the toughening effect of the chain extender on the pCBT matrix. Drop weight impact tests revealed that the energy absorption of the modified composites was relatively higher as compared to unmodified pCBT composites. POLYM. COMPOS., 37:1453–1460, 2016. © 2014 Society of Plastics Engineers     

Toughened epoxy resin matrix for a membrane shell by wet filament winding

A toughened epoxy resin matrix was obtained with a reactive toughening agent and methyl hexahydrophthalic anhydride as a curing agent. The mechanical properties of the modified epoxy resin and its glass‐fiber‐reinforced composites were investigated systematically. The modified epoxy resin matrix possessed many good properties, including a high flexural strength (138 MPa), high elongation at break (5.2%), low viscosity, long pot life at room temperature, and good water resistance. In addition, the glass‐fiber‐reinforced composites showed a high strength conversion ratio of the glass fiber (86.7%) and good fatigue resistance. The results demonstrated that the modified epoxy resin matrix is very suitable for applications in reverse osmosis membrane shell products fabricated with wet filament winding for water treatment. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Bamboo fiber reinforced polypropylene composites and their mechanical,thermal, and morphological properties

Short bamboo fiber reinforced polypropylene composites were prepared by incorporation of various loadings of chemically modified bamboo fibers. Maleic anhydride grafted polypropylene (MA‐g‐PP) was used as compatibilizer to improve fiber–matrix adhesion. The effects of bamboo fiber loading and modification of the resin on the physical, mechanical, thermal, and morphological properties of the bamboo reinforced modified PP composites were studied. Scanning electron microscopy studies of the composites were carried out on the interface and fractured surfaces. Thermogravimetric analysis and IR spectroscopy were also carried out. At 50% volume fraction of the extracted bamboo fiber in the composites, considerable increase in mechanical properties like impact, flexural, tensile, and thermal behavior like heat deflection temperature were observed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

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.     

Effect of structure on mechanical properties of vinyl ester resins and their glass fiber‐reinforced composites

The article describes the effect of structure of vinyl ester resins (VE) on the mechanical properties of neat sheets as well as glass fabric‐reinforced composites. Different samples of VE were prepared by reacting ester of hexahydrophthalic anhydride (ER) and methacrylic acid (MAA) (1 : 1 molar ratio) followed by reaction of monomethacrylate terminated epoxy resin with glutaric (E) or adipic (F) or sebacic acid (G) (2 : 1 molar ratio). The neat VE were diluted with styrene and sheets were fabricated by using a glass mold. A significant reduction in the mechanical properties was observed by increasing the methylene content of resin backbone (i.e., sample E to G). Glass fabric‐reinforced composites were fabricated by vacuum assisted resin transfer molding (VARTM) technique. Resin content in the laminates was 50 ± 5 wt %. Increase in the number of methylene groups in the vinyl ester resin (i.e., increasing the bridge length) did not show any significant effect on limiting oxygen index (LOI) value (21 ± 1) of the laminates but tensile strength, tensile modulus, flexural strength, and flexural modulus all increased though these values are significantly lower than observed in laminates based on resin B. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Surface modification of polyimide fibers by novel alkaline–solvent hydrolysis to form high‐performance fiber‐reinforced composites

We modified polyimide (PI) fibers by a novel hydrolysis approach and fabricated PI‐fiber‐reinforced novolac resin (NR) composites with enhanced mechanical properties. We first used an alkaline–solvent mixture containing potassium hydroxide liquor and dimethylacetamide (DMAc) for the surface modification of the PI fibers. The results indicate that the surface roughness and structure of the PI fibers were controlled by the hydrolysis time and the content of DMAc. With the optimized hydrolysis conditions, the tensile modulus of modified PI fibers improved 15% without compromises in the fracture stress, fracture strain, or thermal stability. The interfacial shear strength between the modified PI fibers and NR increased 57%; this indicated a highly enhanced interfacial adhesion. Finally, the tensile and flexural strengths of the composites increased 72 and 53%, respectively. This research provides an effective method for the surface modification of PI fibers and expands their applications for high‐performance composites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46595.     

Mechanical properties of poly(styrene‐co‐acrylonitrile)‐modified epoxy resin/glass fiber composites

Poly(styrene‐co‐acylonitrile) was used to modify diglycedyl ether of bisphenol‐A type epoxy resin cured with diamino diphenyl sulfone and the modified epoxy resin was used as the matrix for fiber‐reinforced composites (FRPs) to get improved mechanical properties. E‐glass fiber was used as fiber reinforcement. The tensile, flexural, and impact properties of the blends and composites were investigated. The blends exhibited considerable improvement in mechanical properties. The scanning electron micrographs of the fractured surfaces of the blends and tensile fractured surfaces of the composites were also analyzed. The micrographs showed the influence of morphology on the properties of blends. Results showed that the mechanical properties of glass FRPs increased gradually upon fiber loading. Predictive models were applied using various equations to compare the mechanical data obtained theoretically and experimentally. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Influence of fiber modification on interfacial adhesion and mechanical properties of pineapple leaf fiber‐epoxy composites

Three kinds of surface treatment, that is, the alkalization (5% w/v NaOH aqueous solution), the deposition of diglycidyl ether of bisphenol A (DGEBA) from toluene solution (1% w/v DGEBA), and the alkalization combined with the deposition of DGEBA (5% w/v NaOH/1% w/v DGEBA) were applied to modify interfacial bonding and to enhance mechanical properties of pineapple leaf fiber (PALF) reinforced epoxy composites. The fiber strength and strain were measured by single fiber test and the fiber strength variation was assessed using Weibull modulus. Furthermore, a fragmentation test was used to quantify the interfacial adhesion of PALF‐epoxy composite. It was verified that the interfacial shear strength of modified PALFs was substantially higher than that of untreated PALF by almost 2–2.7 times because of the greater interaction between the PALFs and epoxy resin matrix. The strongest interfacial adhesion was obtained from the fibers that had been received the alkalization combined with DGEBA deposition. Moreover, the flexural and impact properties of unidirectional PALF‐epoxy composites were greatly enhanced when reinforced with the modified PALFs due to an improvement in interfacial adhesion, particularly in the synergetic use of 5% NaOH and 5% NaOH/1% DGEBA. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

香蕉纤维的表面改性及其增强环氧树脂复合材料的性能研究

采用硅烷偶联剂(A-174)偶联、高锰酸钾接枝和乙酰化包覆等3种方法对香蕉纤维进行表面改性,制备了改性香蕉纤维增强环氧树脂复合材料,测试其拉伸、弯曲、压缩、冲击等力学性能。结果表明,偶联、接枝、包覆等表面改性均能明显改善香蕉纤维与基体树脂的相容性,提高复合材料的力学性能,其中偶联改性的效果最好。当改性香蕉纤维含量为10wt%时,与未改性的香蕉纤维比较,复合材料的拉伸强度、弯曲强度、压缩强度分别提高了1.8、1.0、2.6倍;随着纤维含量的增加,复合材料的力学性能明显提高。     

Improving delamination resistance of carbon fiber reinforced polymeric composite by interface engineering using carbonaceous nanofillers through electrophoretic deposition: An assessment at different in-service temperatures

In this article, modification of carbon fiber surface by carbon based nanofillers (multi-walled carbon nanotubes [CNT], carbon nanofibers, and multi-layered graphene) has been achieved by electrophoretic deposition technique to improve its interfacial bonding with epoxy matrix, with a target to improve the mechanical performance of carbon fiber reinforced polymer composites. Flexural and short beam shear properties of the composites were studied at extreme temperature conditions; in-situ cryo, room and elevated temperature (−196, 30, and 120°C respectively). Laminate reinforced with CNT grafted carbon fibers exhibited highest delamination resistance with maximum improvement in flexural strength as well as in inter-laminar shear strength (ILSS) among all the carbon fiber reinforced epoxy (CE) composites at all in-situ temperatures. CNT modified CE composite showed increment of 9% in flexural strength and 17.43% in ILSS when compared to that of unmodified CE composite at room temperature (30°C). Thermomechanical properties were investigated using dynamic mechanical analysis. Fractography was also carried out to study different modes of failure of the composites.     

Enzyme‐mediated surface modification of jute and its influence on the properties of jute/epoxy composites

Surface modification of jute fibers is necessary to improve the adhesion and interfacial compatibility between fibers and resin matrix before using fibers in polymer composites. In this study, dodecyl gallate (DG) was enzymatically grafted onto the jute fiber by laccase to endow the fiber with hydrophobicity. A hand lay‐up technique was then adopted to prepare jute/epoxy composites. Contact angle and wetting time measurements showed that the surface hydrophobicity of the jute fabric was increased after the enzymatic graft modification. The water absorption and thickness swelling of the DG‐grafted jute fabric/epoxy composite were lower than those of the other composites. The tensile and dynamic mechanical properties of the jute/epoxy composites were enhanced by the surface modification. Scanning electron microscopy images revealed stronger fiber–matrix adhesion in composites with modified fibers. Therefore, the enzymatic graft modification increased the fiber–matrix interface area. The fiber–matrix adhesion was enhanced, and the mechanical properties of the composites were improved. POLYM. COMPOS., 38:1327–1334, 2017. © 2015 Society of Plastics Engineers     

Mechanical and anticorrosion properties of furan/epoxy‐based basalt fiber‐reinforced composites

A furan/epoxy blend applicable to composite manufacture was studied and corresponding basalt fiber‐reinforced composites were prepared. The processability, mechanical properties, and reasons for the improved mechanical properties of this blend were investigated by rheology machine, mechanical testing machine, and scanning electron microscopy. With excellent processability, furan/epoxy was suitable for manufacturing composites. Furan/epoxy with the ratio of 5/5 showed the best properties, and the impact strength, flexural strength and flexural modulus were 15.43 kJ/m², 102.81 MPa, and 3209.40 MPa, respectively. The river‐like fracture surface of the furan/epoxy system was well consistent with the mechanical properties. The mechanical and anti‐corrosive properties of basalt fiber‐reinforced furan/epoxy composites were also studied. The mechanical properties of composites changed the same as those of furan/epoxy matrix did. Furan resin effectively improved the anti‐acid but not anti‐alkali property of composites, probably because furan could be cured in acidic condition and basalt fiber was resistant to acid and alkali. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44799.     

液体端羧基丁腈橡胶改性氰酸酯／玻璃纤维复合材料的性能研究

用液体端羧基丁腈橡胶(CTBN)对氰酸酯树脂(CE)进行了增韧改性,通过树脂体系的凝胶时间曲线和DSC曲线确定了体系的固化工艺,并制备了玻璃纤维(GF)增强复合材料。CTBN改性后的CE树脂及复合材料具有良好的力学性能,其中固化树脂的弯曲强度和冲击强度分别提高了34.6%和48%,复合材料的弯曲强度和冲击强度分别提高了11.4%和21.3%,这来源于CTBN对氰酸酯树脂的增韧作用及与GF良好的粘接性能。     

Mechanical,thermal, and morphological properties of maleic anhydride‐g‐polypropylene compatibilized and chemically modified banana‐fiber‐reinforced polypropylene composites

Composites were prepared with chemically modified banana fibers in polypropylene (PP). The effects of 40‐mm fiber loading and resin modification on the physical, mechanical, thermal, and morphological properties of the composites were evaluated with scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Infrared (IR) spectroscopy, and so on. Maleic anhydride grafted polypropylene (MA‐g‐PP) compatibilizer was used to improve the fiber‐matrix adhesion. SEM studies carried out on fractured specimens indicated poor dispersion in the unmodified fiber composites and improved adhesion and uniform dispersion in the treated composites. A fiber loading of 15 vol % in the treated composites was optimum, with maximum mechanical properties and thermal stability evident. The composite with 5% MA‐g‐PP concentration at a 15% fiber volume showed an 80% increase in impact strength, a 48% increase in flexural strength, a 125% increase in flexural modulus, a 33% increase in tensile strength, and an 82% increase in tensile modulus, whereas the heat deflection temperature increased by 18°C. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation and characterization of chemically modified Jute–Coir hybrid fiber reinforced epoxy novolac composites

In this study, the effects of fiber surface modification and hybrid fiber composition on the properties of the composites is presented. Jute fibers are cellulose rich (>65%) modified by alkali treatment, while the lignin rich (>40%) coconut coir fibers consist in creating quinones by oxidation with sodium chlorite in the lignin portions of fiber and react them with furfuryl alcohol (FA) to create a coating around the fiber more compatible with the epoxy resins used to prepare polymer composites. The maximum improvement on the properties was achieved for the hybrid composite containing the jute–coir content of 50 : 50. The tensile and flexural strength are recorded as 25 and 63 MPa at modified coir fiber content of 50 vol %, respectively, which are 78% and 61% higher than those obtained for unmodified fiber reinforced composites, i.e., tensile and flexural strength are 14 and 39 MPa, respectively. The reinforcement of the modified fiber was significantly enhanced the thermal stability of the composites. SEM features correlated satisfactorily with the mechanical properties of modified fiber reinforced hybrid composites. SEM analysis and water absorption measurements have confirmed the FA-grafting and shown a better compatibility at the interface between chemically modified fiber bundles and epoxy novolac resin. Hailwood–Horrobin model was used to predict the moisture sorption behavior of the hybrid composite systems. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Hygrothermal cycling effects on the durability of phenolic based composites

Work has been performed to investigate the thermal and mechanical properties of carbon fiber/phenolic resin composites as engineering materials for the aerospace industry. These materials are cost effective while displaying excellent temperature and fire resistance as well as good mechanical properties. All phenolic and epoxy composite specimens used here were prepared by resin transfer molding (RTM) to model a cost‐effective process. Hygrothermal cycling effects on the property changes of phenolic composites were evaluated through thermal, mechanical, and morphological tests. The fracture performance of a phenolic composite modified with a silicone‐based additive decreased after fewer hygrothermal cycles than unmodified phenolic and epoxy composites. Results from dynamic mechanical analysis (DMA) experiments showed that the modified phenolic composite was more significantly affected by the hygrothermal cycling than the unmodified phenolic composites. Fatigue tests showed that the phenolic composites that were not exposed to hygrothermal cycling had more resistance to fatigue cycles than the epoxy composites.     

Blends of poly(ethylene terephthalate) and epoxy as matrix material for continuous fibre reinforced composites

Abstract

The morphology and mechanical properties of poly(ethylene terephthalate) (PET)–epoxy blends and the application of these blends in continuous glass fibre reinforced composites have been investigated. Epoxy resin was applied as a reactive solvent for PET to obtain homogeneous solutions with a substantially decreased melt viscosity. The epoxy resin in these solutions was cured using an amine hardener according to two different schedules. In the first, high temperature curing at 260°C preceded low temperature crystallisation of the PET at 180°C. In the second, the PET was allowed to crystallise prior to low temperature curing at 180°C. After cure, all blends revealed a phase separated morphology of dispersed epoxy in a continuous PET matrix. The flexural strength and failure strain of all cured blends showed an increase with increasing epoxy content, whereas the high temperature cured blends exhibited overall lower flexural properties than those cured at the lower temperature. Microstructural analysis and flexural properties of continuous glass fibre reinforced PET–epoxy laminates showed that the composites obtained had a low void content. These PET–epoxy laminates had increased inplane shear strength in comparison with unmodified PET based laminates, indicating considerably increased fibre–matrix adhesion.     

Sepiolite‐reinforced epoxy nanocomposites: Thermal,mechanical, and morphological behavior

A bisphenol A‐based epoxy resin was modified with pristine sepiolite and an organically surface‐modified sepiolite and thermally cured using two different curing agents: an aliphatic and a cycloaromatic diamine. The nanocomposites were characterized by dynamic mechanical analysis (DMA), rheology, thermogravimetric analysis (TGA), and electron microscopy. The initial sepiolite–epoxy mixtures show a better dispersion for the sepiolite‐modified system that forms a percolation network structure. Mechanical properties have also been determined. The flexural modulus of the epoxy matrix slightly increases by the incorporation of the organophilic sepiolite. The flexural strength of the sepiolite‐modified resin cured with the aliphatic diamine increased by 10%, while the sepiolite‐modified resin cured with the cycloaromatic diamine resulted in a lower flexural strength, as compared with the unmodified resin. Electron micrographs revealed a better nanodispersion of the sepiolite in the epoxy matrix for the organophilic modified sepiolite nanocomposite. The initial thermal decomposition temperature did not change significantly with the addition of sepiolite, whereas mechanical properties were affected. The reduced flexural strength was attributed to the stress concentrations caused by the sepiolite modifier. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Study on interfacial properties of unidirectional flax/vinyl ester composites: Resin manipulation on vinyl ester system

Flax fibers are widely used as reinforcements in bio‐based polymer matrix composites. This study investigated the hydrophilic nature and surface purity of flax fiber that affects fiber/matrix adhesion in combination with hydrophobic structural polymers via matrix modification and the utilization of fiber treatment, specifically in a flax/vinyl ester (VE) composite. A new method to manipulate the vinyl ester system with acrylic resin (AR) was developed to produce flax reinforced. On the other hand, different types of chemical and physical treatments were applied on the flax fiber. FTIR was applied to evaluate the effects of surface treatments. Dynamic mechanical analysis (DMA) was used to analyze the unmodified and modified VE resin system. The surface of untreated and treated flax fibers and their composites were analyzed by scanning electronic microscopy (SEM). Sodium ethoxide‐treated flax/VE with 1% (wt) AR caused the best mechanical performance among all the flax/VE composites evaluated. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

玻纤增强ABS复合材料的制备及性能

以丙烯腈-丁二烯-苯乙烯共聚物(ABS)及玻璃纤维(GF)为原料,以环氧树脂作为界面相容剂,研究了界面相容剂对玻璃纤维增强ABS复合材料力学性能及界面粘接的影响.结果表明:加入环氧树脂,玻纤增强ABS复合材料的力学性能明显提高;随着玻纤质量分数的增加,复合材料的拉伸强度、弯曲强度、冲击强度均逐渐增加;玻纤质量分数为30%时,GF/ABS/环氧树脂复合材料的拉伸强度比未改性的复合材料的拉伸强度提高了30%,弯曲强度提高了25%,冲击强度也提高了50%.