Tensile tests of phenol formaldehyde glass‐powder‐reinforced composites: Pilot study

Phenol formaldehyde was filled with glass powder (GP) to optimize the strength and impact toughness of the composite for structural applications by a research center at the University of Southern Queensland. To reduce costs, the center wished to fill as much of the glass microspheres as possible to maintain sufficient strength and impact toughness in the composites in structural applications. In this project, we varied the weight percentages of the GP in the composites, which were then subjected to tensile tests. The best weight percentage of GP that could be added to the phenolic resin to give the optimum yield, tensile strengths, Young's modulus, and cost was found to be about 10%. The contribution of this study was the finding that if the tensile properties are the most important factors to be considered in the applications of the composites, GP is not a suitable filler. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Moisture sorption of a three‐dimensional braided carbon fiber–epoxy composite under different media

A three‐dimensional braided carbon fiber–epoxy (C_3D/EP) composite was prepared by the vacuum‐assisted resin transfer molding (VARTM) technique. Its moisture absorption behavior under different media was characterized and compared with a unidirectional composite. Similar to the unidirectional composite, diffusion in the 3D composite obeys Fick's second law of diffusion when immersed in distilled water and phosphate‐buffered saline. In HCl and NaOH solutions, no Fickian behavior was observed. The similarity between the unidirectional and 3D composites suggests that fiber structure does not change diffusion pattern. However, the two composites showed different diffusion parameters (k, D, and M_e) in each medium studied. The 3D composite showed lower k, D, and M_e values because of its stronger hindrance effect to transport of moisture molecules. Diffusion in PBS is slower than that in distilled water because of the presence of heavy ions, but the diffusion pattern remains unchanged. In HCl, the diffusion behavior of the two composites cannot be described by Fick's law. In addition, the k value calculated from the initial linear part of the moisture sorption curve is much lower than that in distilled water. Diffusion in NaOH is unusual; the uptake initially increases rather rapidly but quickly drops, which is likely caused by the extensive solubility of the polymer matrix. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 507–512, 2005     

Dynamic mechanical properties of three‐component composites (acrylic polymer/epoxy/SiO2) in the glass‐transition region

In previous studies, we reported the linear and nonlinear rheological properties of three‐component composites consisting of acrylic polymer (AP), epoxy resin (EP), and various SiO₂ contents (AP/EP/SiO₂) in the molten state. In this study, the dynamic mechanical properties of AP/EP/SiO₂ composites with different particle sizes (0.5 and 8 μm) were investigated in the glass‐transition region. The EP consisted of three kinds of EP components. The α relaxation due to the glass transition shifted to a higher temperature with an increase in the volume fraction (?) for the AP/EP/SiO₂ composites having a particle size of 0.5 μm, but the α relaxation scarcely shifted for the composite having a particle size of 8 μm as a general result. This result suggested that the SiO₂ nanoparticles that were 0.5 μm in size adsorbed a lot of the low‐glass‐transition‐temperature (T_g) component because of their large surface area. The AP/SiO₂ composites did not exhibit a shift in T_g; this indicated that the composite did not adsorb any component. The modulus in the glassy state (E′_g) exhibited a very weak &phis; dependence for the AP/EP/SiO₂ composites having particle sizes of 0.5 and 8 μm, although E′_g of the AP/SiO₂ composites increased with &phis;. The AP/EP/SiO₂ composites exhibited a peculiar dynamic mechanical behavior, although the AP/SiO₂ composites showed the behavior of general two‐component composites. Scanning electron microscopic observations indicated that some components in the EP were adsorbed on the surface of the SiO₂ particles. We concluded that the peculiar behavior of the AP/EP/SiO₂ composites was due to the selective adsorption of the EP component. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40409.     

Barrier properties for short‐fiber‐reinforced epoxy foams

The barrier properties of short‐fiber‐reinforced epoxy foam are characterized and compared with unreinforced epoxy foam in terms of moisture absorption, flammability properties, and impact properties. Compression and shear properties are also included to place in perspective the mechanical behavior of these materials. Compared with conventional epoxy foam, foam reinforced with aramid fibers exhibits higher moisture absorption and lower diffusion, while glass‐fiber‐reinforced foam is significantly stiffer and stronger. In addition, the polymeric foam composites studied present superior fire‐resistance compared with conventional epoxy foam systems. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3266–3272, 2006     

Synthesis,fabrication, mechanical,electrical, and moisture absorption study of epoxy polyurethane–jute and epoxy polyurethane–jute–rice/wheat husk composites

Bisphenol‐C‐epoxy‐toluene diisocyanate polyurethane (PEBCT) has been synthesized and used for the fabrication of jute, jute–rice husk (JRH), and jute–wheat husk (JWH) composites. The composites have been fabricated by hand lay‐up technique under a hydraulic pressure of 30.4 MPa at 135°C for 2.5 h. PEBCT‐J, PEBCT‐JRH, and PEBCT‐JWH possess respectively, tensile strength of 37.4, 9.5, and 14.7 MPa, and flexural strength of 39.6, 12.9, and 21.3 MPa, electric strength of 1.3, 1.8, and 1.9 kV/mm and volume resistivity of 1.40 × 10¹³, 1.84 × 10¹³, and 1.91 × 10¹³ ohm cm. Tensile strength and flexural strength have decreased, while electric strength and volume resistivity are improved upon hybridization. PEBCT‐JWH has better interfacial bond strength and stiffness as compared to PEBCT‐JRH. Moisture uptake behavior of PEBCT‐J in water, 10% HCl and 10% NaCl at room temperature is quite different. Equilibrium moisture content of PEBCT‐J in 10% NaCl (5.5%) is almost half of those in water (11.3%) and 10% HCl (13.6%) environments. Equilibrium time for saline environment is also comparatively low. Equilibrium moisture uptake in boiling water has increased 1.84 times, while equilibrium time has decreased 15.3 times. The composites may be useful for low load bearing in construction industries and for marine applications. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Process–structure–property relationship in ternary short‐glass‐fiber/elastomer/polypropylene composites

Short‐glass‐fiber (SGF)‐reinforced polypropylene (PP) composites toughened with a styrene/ethylene butylene/styrene (SEBS) triblock copolymer were injection molded after extrusion. Furthermore, a maleic anhydride (MA)‐grafted SEBS copolymer (SEBS‐g‐MA) was used as an impact modifier and compatibilizer. The effects of the processing conditions and compatibilizer on the microstructure and tensile and impact performance of the hybrid composites were investigated. In the route 1 fabrication process, SGF, PP, and SEBS were blended in an extruder twice, and this was followed by injection molding. In route 2, or the sequential blending process, the elastomer and PP were mixed thoroughly before the addition of SGF. In other words, either PP and SEBS or PP and SEBS‐g‐MA pellets were premixed in an extruder. The produced pellets were then blended with SGF in the extruder, and this was followed by injection molding. The SGF/SEBS‐g‐MA/PP hybrid fabricated by the route 2 process exhibited the highest modulus, yield stress, tensile stress at break, Izod impact energy, and Charpy drop weight impact strength among the composites investigated. This was due to the formation of a homogeneous SEBS elastomeric interlayer at the SGF and matrix interface of the SGF/SEBS‐g‐MA/PP hybrid. This SEBS rubbery layer enhanced the interfacial bonding between SGF and the matrix of the SGF/SEBS‐g‐MA/PP hybrid. The correlations between the processing, microstructure, and properties of the hybrids were investigated. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1384–1392, 2003     

Mechanical and dielectric properties of short‐carbon‐fibers/epoxy‐modified‐organic‐silicone‐resin as heat resistant microwave absorbing coatings

Heat resistant microwave absorbing coatings were prepared by brushing and thereafter heat treatment, using epoxy modified organic silicone resin as binding material, short carbon fibers (C_sf) as absorbers, talcum powder and glass powder as filling materials. The mechanical and dielectric properties of the coatings before and after heat treatment at 600°C for 10 mins were studied. The results showed that the adhesive power after heat treatment enhances remarkably, both the real (ε′) and imaginary (ε″) parts of the permittivity of the coatings increase with increasing C_sf content in the frequency range of 8.2–12.4 GHz. The calculation value of the reflection loss as single layer absorber indicates that epoxy modified organic silicone resin coatings containing short carbon fibers could be a promising radar absorbing material applied at high temperature. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 1392‐1398, 2013     

Investigation of mechanical properties of alumina nanoparticle‐loaded hybrid glass/carbon‐fiber‐reinforced epoxy composites

This research work investigates the tensile strength and elastic modulus of the alumina nanoparticles, glass fiber, and carbon fiber reinforced epoxy composites. The first type composites were made by adding 1–5 wt % (in the interval of 1%) of alumina to the epoxy matrix, whereas the second and third categories of composites were made by adding 1–5 wt % short glass, carbon fibers to the matrix. A fourth type of composite has also been synthesized by incorporating both alumina particles (2 wt %) and fibers to the epoxy. Results showed that the longitudinal modulus has significantly improved because of the filler additions. Both tensile strength and modulus are further better for hybrid composites consisting both alumina particles and glass fibers or carbon fibers. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39749.     

Preparation and evaluation of nano‐epoxy composite resins containing electrospun glass nanofibers

In this study, electrospun glass (structurally amorphous SiO₂) nanofibers (EGNFs) with diameters of ～ 400 nm were incorporated into epoxy resin for reinforcement and/or toughening purposes; the effects of silanization treatment (including different functional groups in silane molecules) and mass fraction of EGNFs on strength, stiffness, and toughness of the resulting nano‐epoxy composite resins were investigated. The experimental results revealed that EGNFs substantially outperformed conventional glass fibers (CGFs, with diameters of ～ 10 μm) in both tension and impact tests, and led to the same trend of improvements in strength, stiffness, and toughness at small mass fractions of 0.5 and 1%. The tensile strength, Young's modulus, work of fracture, and impact strength of the nano‐epoxy composite resins with EGNFs were improved by up to 40, 201, 67, and 363%, respectively. In general, the silanized EGNFs with epoxy end groups (G‐EGNFs) showed a higher degree of toughening effect, while the silanized EGNFs with amine end groups (A‐EGNFs) showed a higher degree of reinforcement effect. The study suggested that electrospun glass nanofibers could be used as reinforcement and/or toughening agent for making innovative nano‐epoxy composite resins, which would be further used for the development of high‐performance polymer composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of an epoxy‐based bonding agent on the cure characteristics and mechanical properties of short‐nylon‐fiber‐reinforced acrylonitrile–butadiene rubber composites

The cure characteristics and mechanical properties of short‐nylon‐fiber‐reinforced acrylonitrile–butadiene rubber composites with and without an epoxy resin as a bonding agent were studied. The epoxy resin was a good interfacial‐bonding agent for this composite system. The minimum torque showed a marginal increase with the resin concentration. The maximum–minimum torque showed only a marginal change with the resin. The scorch time decreased with the fiber concentration and resin content. The tensile strength and abrasion resistance were improved and the tear resistance and resilience were reduced with the resin concentration. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 532–539, 2006     

Mechanical and tribological properties of glass–epoxy composites with and without graphite particulate filler

The objectives of this research article is to evaluate the mechanical and tribological properties of glass‐fiber‐reinforced epoxy (G–E) composites with and without graphite particulate filler. The laminates were fabricated by a dry hand layup technique. The mechanical properties, including tensile strength, tensile modulus, elongation at break, and surface hardness, were investigated in accordance with ASTM standards. From the experimental investigation, we found that the tensile strength and dimensional stability of the G–E composite increased with increasing graphite content. The effect of filler content (0–7.5 wt %) and sliding distance on the friction and wear behavior of the graphite‐filled G–E composite systems were studied. Also, conventional weighing, determination of the coefficient of friction, and examination of the worn surface morphological features by scanning electron microscopy (SEM) were done. A marginal increase in the coefficient of friction with sliding distance for the unfilled composites was noticed, but a slight reduction was noticed for the graphite‐filled composites. The 7.5% graphite‐filled G–E composite showed a lower friction coefficient for the sliding distances used. The wear loss of the composites decreased with increasing weight fraction of graphite filler and increased with increasing sliding distance. Failure mechanisms of the worn surfaces of the filled composites were established with SEM. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2472–2480, 2007     

Modification of dry‐spun Suplon polyimide fibers by mixed‐acid oxidation and their effects on the properties of polypropylene‐resin‐based composites

In this study, the effects of mixed‐acid oxidation on the contents of surface elements, morphology, fiber fineness, mechanical properties, mass change rate, chemical structure, and microaggregate structure of dry‐spun Suplon polyimide (PI) fibers were systematically investigated with wet chemical treatment with HNO₃/H₂SO₄. Experiments investigating both the improvement in the O/C ratio of the fiber surface elements and the changes in other performance features were conducted through the functional modification of the fibers. Meanwhile, the causes of specific changes in the mechanical properties of the oxidized PI‐fiber‐reinforced polypropylene‐resin‐based composites were studied and are discussed. The results of this study demonstrate that the treatment of the fibers with HNO₃/H₂SO₄ mixed‐acid oxidation resulted in significant changes in the properties of the fibers; these changes included an uneven surface, increased specific surface area and surface roughness, a locally etched surface, increased surface energy and O/C ratio, an enhanced wettability, an increased fiber fineness, reduced mechanical properties, and a mass gain in the fibers. Although the chemical structures of the fibers treated by oxidized HNO₃/H₂SO₄ were not significantly changed compared to those of the untreated fibers, the microscopic aggregation of the treated fibers changed to some degree, and the ratio of the amorphous regions significantly increased. Taken together, the functional modification of the PI fiber surface was achieved efficiently through the use of a suitable HNO₃/H₂SO₄ oxidation process and with other performance features of the fibers taken into account. This was favorable for the enhancement of the interfacial properties of the polypropylene fibers and the matrix resins, and thus, the modification improved the mechanical properties of the composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44932.     

Properties of epoxy molding compound according to the pretreatment method of an amino‐silane coupling agent on epoxy or phenol resin

An amino‐functional silane coupling agent, which is an important component for epoxy molding compound (EMC), has been used by diverse methods, such as integral addition into a mixed powder and pretreatment on silica or on resin. However, the homogeneous dispersion of the amino‐functional silane coupling agent in mixed powder is limited with integral addition, and the possibility of white gel formation, sometimes causing gate blocking during the transfer‐molding process, due to the aggregation of silica with the coupling agent cannot be completely removed by it. The pretreatment of the amino‐functional silane coupling agent on silica has been adopted as an alternative process, but the process is expensive and limited in mass production. Although the pretreatment of the coupling agent on resin as another method has also been used by some EMC manufacturing companies, it has hardly been known in which resin phase, the epoxy or hardener, the silane coupling agent should be pretreated for better mechanical properties of EMC. In this study, the pretreatment of the amino‐functional silane coupling agent on epoxy or phenol resin, essential components of EMC, has been investigated with respect to the reaction during the pretreatment and the properties of EMC according to the different pretreatment methods. In the case of the pretreatment on epoxy, the amino‐functional silane coupling agent rapidly forms an adduct with epoxy via a ring‐opening reaction, whereas its alkoxy groups are well preserved. The glass‐transition temperature and flexural strength of the EMC by the application of the pretreatment method on epoxy are lower than those by the pretreatment on phenol. It is thought that the degree of linkage between the resin matrix and silica becomes lower because of the confinement of aminopropyltriethoxy silane (APTS) within the epoxy matrix through an irreversible reaction with epoxy in advance. In the case of the pretreatment on phenol, most of the alkoxy groups in the coupling agent are assumed to be replaced with protonic nucleophiles such as phenol, generating an equivalent amount of alcohol. Because the adduct between the phenol and amino‐functional silane coupling agent can be easily regenerated during the manufacturing process, it is thought that the pretreatment method of APTS on phenol helps APTS disperse well within EMC. Actually, the glass‐transition temperature and flexural strength of EMC by the application of the pretreatment method on phenol are higher than those by the integral addition method and the pretreatment on epoxy. However, they become lower as the degree of reaction of silane with phenol increases. The pretreatment of the amino‐functional silane coupling agent on phenol shows lots of advantages over the previous methods. From the viewpoint of the process, the homogeneous dispersion of the coupling agent can be obtained with consistency, and the possibility of white gel formation can also be completely removed by it. From the perspective of properties, through a controlled pretreatment on phenol resin, better mechanical properties of EMC can be obtained than those through the pretreatment on epoxy. In addition, the pretreatment process on phenol is simple and feasible for mass production. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 2171–2179, 2006     

Processing,structure, and properties of multiwalled carbon nanotube–poly(phenylene sulfide) composite fibers

To improve the processability and properties of the poly(phenylene sulfide) (PPS) fibers at room temperature and high temperatures, a series of composite fibers based on PPS and multiwalled carbon nanotubes were prepared by melt spinning. We researched the processability with a high‐pressure capillary rheometer, and the properties of the composite fibers were investigated in detail by scanning electron microscopy, differential scanning calorimetry, fiber sonic velocity measurement, and single‐fiber strength testing. The results show that the carbon nanotubes (CNTs) had good interfacial adhesion with PPS and dispersed homogeneously in the PPS matrix. When the shear rate was higher than 500 s^?1, the oriented CNTs induced the orientation of PPS molecular chains; this resulted in a decline in the apparent viscosity and an increase in the orientation degree of the molecular chains. Meanwhile, the CNTs acted as nucleating agents to effectively improve the crystallization of PPS. The strength of the fibers at room temperature were improved by 28.8% after the addition of 0.2% CNTs, and the initial modulus was also significantly enhanced. The strength retention at 160 °C was promoted from 60.58 to 88.32% with the addition of 1.0% CNTs. The shrinking percentage decreased to almost zero from higher than 15%; this suggested that the CNTs could efficiently improve the dimensional stability at high temperatures. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44609.     

Simultaneous enhancements in the mechanical,thermal, and electrical performances of glass‐fiber‐reinforced cyanate ester/epoxy composites with plasma‐functionalized carbon nanotubes at different temperatures

Woven glass‐fiber‐reinforced cyanate ester/epoxy composites modified with plasma‐functionalized multiwalled carbon nanotubes (MWCNTs) were prepared. The mechanical, thermal, and electrical properties of the composites were investigated at different temperatures. The results show that the interlaminar shear strength, thermal conductivity, and electrical conductivity of the composites at room temperature and the cryogenic temperatures were enhanced simultaneously by the incorporation of MWCNTs, whereas the nonconductive behavior of the composites as electrical insulating materials was not changed. Meanwhile, the reinforcing mechanism was also examined on the basis of the microstructure of the composites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41418.     

Wood–high‐density polyethylene composites: Water absorption and mechanical properties

In this research, the effect of water absorption on the mechanical properties of wood/high‐density polyethylene (HDPE) composites were investigated. HDPE (44005ARPC) was used as the polymer matrix, and spruce sawdust was used as the filler at a maximum loading of 50 wt % of the total weight of each compound. All compounds contained 5 wt % magnesium stearate as a lubricant and 0.5 wt % Irgafos 168 as a heat stabilizer. Four factors in two levels were chosen [talc (filler) at levels of 5 and 15 wt %, zinc borate (fungicide) at levels of 0 and 1 wt %, maleic anhydride polyethylene (coupling agent) at levels of 4 and 6 wt %, and method of mixing (one‐step vs. two‐step mixing)], and eight compounds were prepared with an L8 Taguchi orthogonal array which has 8 combinations of levels. The effects of each factor at two levels on the diffusion constant and the tensile and bending strengths (under wet and dry conditions) were investigated by the analysis of variance of means with 90% confidence. The optimum level for each factor is reported. The results show that there was a linear correlation between the diffusion constant and tensile and bending strengths when the samples were immersed in distilled water. A higher diffusion constant resulted in much lower tensile and bending strengths with immersion in distilled water until saturation was reached. Scanning electron microscopy images confirmed good mixing when two‐steps mixing was used. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Failure behavior of resorcinol–formaldehyde latex coated aramid short‐fiber‐reinforced rubber sealing under transverse tension

Composites composed of rubber, sepiolite fiber, and resorcinol–formaldehyde latex‐coated aramid short fibers were prepared. Mechanical and morphological characterizations were carried out. To investigate the effect of interfacial debonding on the failure behavior of short‐fiber‐reinforced rubber composites, a micromechanical representative volume element model for the composites was developed. The cohesive zone model was used to analyze the interfacial failure. We found that computational results were in good agreement with the experimental results when the interfacial fracture energy was 1 J/m² and the interfacial strength was 10 MPa. A parametrical study on the interface and interphase of the composite was conducted. The results indicate that a good interfacial strength and a choice of interphase modulus between 40 and 50 MPa enhanced the ductile behavior and strength of the composite. The ductile properties of the composite also increased with increasing interfacial fracture energy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41672.     

Mechanical properties of copper‐clad laminate using composite naphthalene–phenyl‐based epoxy as prepreg

A composite was prepared that contained diglycidyl ether of tetrabromobisphenol A (DGETBA) and 1,5‐di(2,3‐epoxypropoxy)naphthalene (A), 4,4′‐bis(2,3‐epoxypropoxy)benzylideneaniline (B), or 4,4′‐bis(2,3‐epoxypropoxy)biphenyl (C), and then was cured using different ratios of dicyandiamide (DICY). The results of DSC, TGA, coefficient of thermal expansion, dielectric constant, and dissipation factor testing of the composite epoxy resins were analyzed, and investigation of the copper‐clad laminate using the composite epoxy resins as prepreg was also performed. Additionally, moisture absorption, peel strength, arc resistance, comparative tracking index, and flammability of the copper‐clad laminate were examined. Clearly, some of the physical or mechanical properties of the composite and the copper‐clad laminate can be improved by optimal addition of naphthalene–phenyl‐based epoxy. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 95: 1485–1492, 2005     

Mechanical properties of acrylonitrile–butadiene–styrene copolymer/poly(l‐lactic acid) blends and their composites

As the material properties of acrylonitrile–butadiene–styrene copolymer (ABS) have an excessively wide margin for applications in automobile console boxes, ABS partly replaced with poly(l ‐lactic acid) (PLA) may be used for the same purpose with improved ecofriendliness if the corresponding deterioration of the material properties is acceptable through the choice of appropriate additives. ABS composites with 30 wt % renewable components (PLA and cellulose pulp) were prepared by melt compounding, and the material properties were examined as a function of the additive content. The changes in the mechanical properties of the ABS/PLA blends were examined after the addition of cellulose pulp and two clays [Cloisite 25A (C25A) and sodium montmorillonite] as well as these two clays treated with bis(3‐triethoxysilylpropyl)tetrasulfide (TESPT). The heat distortion temperatures of the composites were measured as a function of the content of the TESPT‐treated C25A. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40329.