Influence of processing rate and formulation on the interface strength of vinyl ester/E‐glass composites

The single fiber fragmentation test was used to investigate the effect of gelation time on interfacial shear properties of fast reacting resin systems. We developed a processing system capable of producing single fiber fragmentation samples with gelation times that ranged from 2 min to 45 min. The interfacial properties of E‐glass fibers in vinyl ester resin were measured with single fiber fragmentation tests using a manual and an automated testing machine. We found that vinyl ester resins catalyzed with methyl ethyl ketone peroxide and promoted with cobalt naphthenate and dimethylaniline gelled in less than two minutes and had an estimated interfacial shear strength of 105 MPa. Specimens cured without the promoter gelled in 45 min and had an interfacial shear strength of 72 MPa. Further curing of the unpromoted specimens resulted in an increase in shear strength to 96 MPa. We have demonstrated the ability to make and test rapidly cured specimens, thus expanding the range of materials that can be tested using the single fiber fragmentation testing technique.     

Mode‐I intralaminar fracture toughness of silica particles‐filled glass woven fabric‐reinforced vinyl ester composites

Glass woven fabric reinforced vinyl ester (GV) composites filled with different weight proportions of silica particles were fabricated by hand lay up technique followed by oven curing. The plane strain Mode‐I Intralaminar fracture toughness, K_IC of the silica filled GV composites has been studied and the experimental results were compared with those of unfilled GV composites. The findings of the experiments showed that the fracture toughness has improved by the addition of silica particles up to 6 weight % with marginal increase of tensile properties. The silica filled and unfilled GV composites showed brittle fracture, with maximum toughness for 6 weight % silica particles. The morphology of fracture surfaces was examined by using SEM. Pulled and fractured fibers are observed on the fracture surface of GV composites evidencing fiber bridging but not in the silica filled GV composites. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

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     

Ion‐leaching behaviors and corrosion morphology of glass fiber reinforced vinyl ester composites in sulfuric acid solution

The corrosion mechanism of glass‐fiber reinforced vinyl ester composites was investigated by immersing composite samples in 40 wt% sulfuric acid solution at constant temperature of 35°C, 55°C, 65°C, and 75°C for periods up to 10,500 h. Results were characterized through weight gain tests, inductively coupled plasma analysis, and scanning electron microscope (SEM). Weight gains and ion‐leaching behaviors show that the composite interface has undergone significant changes due to a long corrosive environment, and the interface corrosion of composite increases with increasing the temperature. SEM images of surface and cross‐section of samples indicated that there exit in irreversible degradation reaction on resin matrix and interface in composite, which lead to the increase of weight gain and ion leachability, especially at high temperatures. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Mechanical properties of particulate‐filler/woven‐glass‐fabric‐filled vinyl ester composites

Studies of the effect of particulate fillers on specific mechanical properties of vinyl ester epoxy (VE) reinforced with woven glass fiber composites were carried out with different filler types and particulate filler contents (1%, 3%, and 5% by weight). Two types of particulate filler were used, i.e., calcium carbonate (CC) and phenolic hollow microspheres (PHMS). The composites were prepared by using a hand lay‐up and vacuum bagging method. Woven glass fabric composites filled with particulate PHMS were observed to have better specific flexural strength and specific impact strength, as well as lower density, than those filled with particulate CC. Morphological features determined by scanning electron microscope (SEM) proved that the PHMS filler experienced good bonding in the VE matrix, a feature which contributed to the improvement in the properties of the composites. The incorporation of particulate fillers into the composites also influenced the storage modulus with a minimal effect on T_g. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Novel vinyl ester resin and its urethane derivatives for glass reinforced composites

The paper describes glass-fibre-reinforced composites of a vinyl ester resin derived from triglycidyl-m-aminophenol and its urethane derivatives. The fabricated laminates were characterized by their mechanical properties and chemical resistance. The incorporation of vinyl monomer styrene in the resin system was found to improve some properties of composites remarkably.     

Processing and mechanical properties of bio‐derived vinyl ester resin‐based composites

A “green” vinyl ester resin (GVER) is investigated for use in structural applications. The GVER was formulated using a monodisperse vinyl ester created via a novel synthetic route capable of using bio‐waste material from paper and biodiesel industries. The GVER was used either as a neat resin or as blended with a commercial vinyl ester resin. The processing viscosity and gel times are investigated. The GVER reaches a similar viscosity as the commercial resin with only half the styrene monomer content, thereby reducing the volatile organic compounds associated with manufacturing. Composites of the GVER matrix reinforced by carbon fabric were tested for their tensile and flexural properties. The mechanical performance of the GVER compares favorably with commercial resin and provide a route for composites manufacturing from sustainably sourced vinyl ester matrix. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44642.     

Morphology and mechanical properties of reactive compatibilized polystyrene/ethylene‐vinyl acetate‐vinyl alcohol blends

A reactive compatibilizer, styrene‐maleic anhydride (SMA) was used to compatibilize the blends of polystyrene (PS) and ethylene‐vinyl acetate‐vinyl alcohol (EVAOH), which was synthesized from ethylene‐vinyl acetate (EVA) using transesterification reaction. The compatibilized blends with different compositions were prepared using a twin‐screw extruder and injection molded into the required test specimens. Morphology of Charpy impact‐fractured surfaces, tensile, and impact properties of the blends were investigated. Fourier‐transform infrared spectroscopy (FTIR) was also applied for specific samples to elucidate the presence of the functional groups reaction necessary for reactive compatibilization. The results of the ternary PS/EVAOH/SMA blends illustrate that the addition of SMA as a compatibilizer slightly reduce the elongation at break. From the impact‐fractured surfaces of the blends, it is evident that the morphology developed sizable pores when SMA was added into the blends. This might be attributed to the residual octanol‐1, produced from the synthesis of EVAOH, as there is a possibility of a reaction between hydroxyl groups in the octanol‐1 and the anhydride groups in the SMA. This disrupted the stability of the morphology and resulted in the decrease in the elongation, and hence, the tensile toughness. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 209–217, 2002     

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     

Hybrid carbon-glass fiber vinyl ester resin composites

Hybrid carbon-glass fiber composites of novolak epoxy-based vinyl ester resins have been investigated. The chemical resistance, the thermo-oxidative stability and the mechanical properties such as tensile strength and tensile modulus, as well as flexural strength and flexural modulus, interlaminar shear strength (ILSS) and impact strength have also been estimated. The combination of glass and carbon fibers in the hybrid turns out to be an excellent mix. These composites have good tensile and flexural properties as well as the good chemical resistance of the carbon fibers and the high impact strength of the glass fibers and also the thermo-oxidative stability of highly aromatic vinyl ester resins based on novolak epoxy.     

Simultaneous effects of silanized coal fly ash and nano/micro glass fiber on fracture toughness and mechanical properties of carbon fiber‐reinforced vinyl ester resin composites

In this study, the simultaneous effects of both silanized coal fly ash (S‐CFA) and nano/micro glass fiber (nGF) on fracture toughness and mechanical properties of vinyl ester (VE) resin filled with carbon fiber‐based composite materials were investigated. The CFA was treated with (3‐trimethoxysilyl) propyl methacrylate to introduce the methacryloxy groups into the surface of CFA, and was confirmed by using FTIR technique. The nGF and S‐CFA with different weight ratios were well mixed with VE resin by using of high‐speed mechanical stirrer, and ultrasonic technique before using as matrices for fabrication of carbon fiber‐based composite materials via sheet molding compound (SMC) method and hot curing processing. Many characteristics of both cured VE resin composites and carbon fiber‐based composite were examined such as mechanical properties, fracture toughness, and morphology. The results showed that by adding of both 0.1 wt% nGF and 1 wt% S‐CFA into VE resin the tensile strength, tensile modulus, flexural strength, K_IC, impact strength as well as the Mode I interlaminar fracture toughness (G_IC) of VE composites and carbon fiber based composites get optimum values and increased about 61.39%; 39.83%; 36.21%; 103.1%; 81.79%; 48.61%, respectively when compared with pristine materials. POLYM. ENG. SCI., 59:584–591, 2019. © 2018 Society of Plastics Engineers     

Thermal behavior of vinyl ester resin matrix composites reinforced with alkali‐treated jute fibers

The thermal behavior of vinyl ester resin matrix composites reinforced with jute fibers treated for 2, 4, 6, and 8 h with 5% NaOH was studied with Thermo‐gravimetric analysis and differential scanning calorimetry. The moisture desorption peak shifted to a higher temperature, from 37 to 58.3°C, for all the treated‐fiber composites because of improved wetting of the fibers by the resin and stronger bonding at the interface. The degradation temperature of the vinyl ester resin in the composites was lowered to 410.3°C from that of the neat resin, 418.8°C. The X‐ray diffraction studies showed increased crystallinity of the treated fibers, which affected the enthalpy of the α‐cellulose and hemicellulose degradation. The hemicellulose degradation temperature remained the same (299.7°C) in all the treated‐fiber composites, but the enthalpy associated with the hemicellulose degradation showed an increasing trend in the treated composites with a small increase in the weight loss. This could be attributed to the increased hydrogen bonding between the more accessible ? OH groups of the hemicellulose in the noncrystalline region of the jute fiber and the resin. The degradation temperature of α‐cellulose was lowered from 364.2 to 356.8°C in the treated composites. The enthalpy of α‐cellulose degradation showed a decreasing trend with a lowering of the weight loss. The crystalline regions of the fiber, consisting of closely packed α‐cellulose chains, were bonded with the resin mainly on the surface through hydrogen bonds and became more resistant to thermal degradation; this reduced the weight loss. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 123–129, 2004     

Preparation of boz/glass fibers/cyanate ester resins laminated composites

A novel kind of high performance laminated composites of Bis allyl benzoxazine/Quartz fibers/Cyanate ester (Bz‐ally/QFs/CE) have been developed. The effects of Bz‐ally on the moisture resistance, mechanical, dielectric, and thermal properties of Bz‐ally/QFs/CE laminated composites were investigated systematically. Compared with QFs/CE laminated composites, the flexural strength and the interlaminar shear strength value of the Bz‐ally/QFs/CE laminated composites were improved markedly with up to 25.2% and 22.3% increasing magnitude, respectively. Meanwhile, the Bz‐ally/QFs/CE laminated composites exhibit lower dielectric constant and loss than QFs/CE laminated composites over the testing frequency from 10 to 60 MHz. In addition, the thermal stability and moisture resistance of Bz‐ally/QFs/CE laminated composites were also superior to that of Boz/QFs/CE laminated composites. POLYM. COMPOS., 38:523–527, 2017. © 2015 Society of Plastics Engineers     

Preparation,characterization, and improvement of hollow epoxy particle‐toughened vinyl ester composites for high‐end applications

Spherical hollow epoxy particles (HEPs) that can serve as advanced reinforcing fillers for vinyl ester thermosets were prepared using the water‐based emulsion method. The HEP fillers were incorporated into the vinyl ester matrices at different loading amounts, ranging from 0 to 9 wt %, to reinforce and toughen the vinyl ester composite. The optimum mechanical properties of the HEP‐toughened epoxy composite can be achieved by the addition of 5 wt % HEP filler into the vinyl ester matrices. The toughening and strengthening of the epoxy composites involved the interlocking of vinyl ester resins into the pore regions on the HEP fillers. The toughening and interlocking mechanisms of HEP‐toughened vinyl ester composites were also proposed and discussed. The addition of HEP fillers into vinyl ester matrices increased the glass transition temperature (T_g) and thermal stability of the composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Novel high‐performance wave‐transparent aluminum phosphate/cyanate ester composites

Advanced wave‐transparent composites are the key materials for many cutting‐edge industries including aviation and aerospace, which should have outstanding heat resistance, low dielectric constant and loss as well as good mechanical properties. A novel kind of high‐performance wave‐transparent composites based on surface‐modified aluminum phosphate AlPO₄(KH‐550) and cyanate ester (CE) was first developed. The dielectric and dynamic mechanical properties of AlPO₄(KH‐550)/CE composites were investigated intensively. Results show that AlPO₄(KH‐550)/CE composites have decreased dielectric loss and higher storage moduli than pure CE resin; in addition, the composites with suitable AlPO₄(KH‐550) concentration remain the outstanding thermal property and low dielectric constant of pure CE resin. The reasons attributing to these results are discussed from the effects of AlPO₄(KH‐550) on the key aspects such as morphology, curing mechanism, and interfacial adhesion of composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Thermal characteristics of ethylene‐co‐vinyl acetate/cellulose microfibers composites

Cellulose microfibers were obtained from Hibiscus sabadariffa by steam explosion technique. Structural and surface analysis of the microfibers showed a reduction in diameter and changes in surface morphology from that of raw fibers. The chemical composition of fibers showed increase in α‐cellulose content and decrease in lignin and hemicelluloses for the microfibers. These factors were further confirmed by XRD, SEM, and FTIR results. The CMF were introduced to EVA at different loading by melt extrusion. The composites were analyzed for their thermal stability and phase transition using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA analysis of the composites showed increased onset temperatures for composites compared with pure EVA indicating the superior thermal stability of the composites with fiber loading. DSC analysis shows increase in melting enthalpy and percentage crystallinity with fiber loading increases. Kinetic parameter for the degradation of the composites was obtained using Broido, Coats–Redfern, and Horowitz‐Metzger methods. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Low‐velocity impacts in continuous glass fiber/polypropylene composites

The low‐velocity impact behavior of a continuous glass fiber/polypropylene composite was investigated. Optical microscopy and ultrasonic scanning were used to determine the impact‐induced damage. At low impact energy, the predominant damage mechanism observed was matrix cracking, while at high energy the damage mechanisms observed were delamination, plastic deformation, which produced a residual specimen curvature, and a small amount of fiber breakage at the edge of the indentation on the impacted face of the specimens. The impact load vs. time signals were recorded during impact and showed that the load corresponding to the onset of delamination was independent of the impact energy in the range tested. The load at which the onset of delamination occurred corresponded to the values obtained by performing a linear regression of the delaminated area, obtained by ultrasonic scanning, as a function of the impact force. Tensile and flexural tests performed on impacted specimens showed that the tensile and flexural residual strengths and the flexural modulus decreased with increasing incident impact energy, while the post‐impact residual tensile modulus remained constant. The dynamic interlaminar fracture toughness was evaluated from the critical dynamic (impact) strain energy release rate of specimens with a delamination simulated by an embedded insert. The results are compared with the interlaminar fracture toughness values obtained during subcritical steady crack growth.     

Thermal and combustion behavior of ethylene‐vinyl acetate/aluminum trihydroxide/Fe‐montmorillonite composites

The flammability characterization and synergistic flame‐retardant effect of Fe‐montmorillonite (Fe‐OMT) in the ethylene‐vinyl acetate/aluminum hydroxide (EVA/ATH) compounds were studied using limiting oxygen index (LOI), UL‐94 test, cone calorimeter, microscale combustion calorimetry (MCC), and thermogravimetric analysis (TGA). The results showed that addition of Fe‐OMT increases the LOI value and improves the UL 94 rating. Cone calorimeter data indicate that the addition of Fe‐OMT greatly reduced the heat release rate and carbon monoxide production rate. Furthermore a compact char residue formed on the surface of the sample with a suitable of Fe‐OMT during the combustion. The MCC results indicate that addition of Fe‐OMT reduced the heat release rate and catalyzed the decomposition of EVA. The TGA data showed further evidence that Fe‐OMT can catalyze carbonization reactions. POLYM. ENG. SCI., 2012. © 2011 Society of Plastics Engineers     

Thermophysical properties of composites formed from ethylene–vinyl acetate copolymer and silver‐coated hollow glass microspheres

The primary purpose of this study was to prepare a new type of silver‐coated hollow glass microspheres and to make available this facility for the fabrication of thermally conductive polymeric composites based on ethylene–vinyl acetate (EVA) copolymer. Thermally conducting composites could be produced with a silver coating around the hollow glass microspheres, despite the low silver volume content. The experimental results are discussed and compared to various theoretical models. The thermal diffusivity and the specific heat of the composites were also characterized and are reported. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Comparing reinforcement strategies for epoxy networks using reactive and non‐reactive fortifiers

Improvements in physical, mechanical, and thermal properties of an epoxy network are made with the use of a unique class of molecules that reinforce the network at the molecular scale. These molecules are commonly referred to as antiplasticizers or fortifiers. In this contribution, two types of fortifiers are incorporated into the model epoxy network. One, dimethyl methylphosphonate, is a simple additive while the other, diethyl phosphoramidate, contains a reactive amine and is cured as part of the network. The two approaches provide some unique differences in the physical and mechanical properties of the networks. Several mechanisms of fortification are discussed and correlated to the observed properties. In addition, it is shown that the fortifiers improve the rheological characteristics of the epoxy resin and act as fire‐retardants in the cured network. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4606–4615, 2006