Prefailure damage processes in highly filled glass/mica/epoxy composites

In the present study, the prefailure damage processes of a series of short glass fiber/mica/epoxy composites under three-point bending were elucidated using acoustic emission (AE) coupled with in situ scanning electron microscopy (SEM) observations. This study consisted of a detailed investigation of the damage tolerance of composite systems that had constant inorganic content of 75% by weight with a varying ratio of glass fibers to mica. The flexural strength was found to increase from 11 to 21 ksi as the glass fiber content increased (mica content decreased), while the flexural modulus decreased from 5.0 to 2.5 Msi. By monitoring the AE during flexural deformation of the glass fiber-to-mica ratio composites, it was determined that low amplitude (0–42 db) AE events, which occurred throughout the deformation process, were caused by matrix cracking, whereas the high-amplitude (43–100 db) AE events, which occurred just prior to failure, were caused by a fiber-related mechanism. In situ SEM observations of the composites during flexural deformation allowed a correlation between the AE and the damage mechanisms as a function of strain. In the all-mica composite, microcracking initiated in the linear region at preexisting flaws, on the order of 10 μm, located at the mica interface. These microcracks grew along the mica contours over the majority of the deformation process, emitting low-amplitude events, until final fracture occurred at relatively low strains. In the glass fiber-containing composites, microcracking initiated in the linear region at preexisting flaws and voids, on the order of 10 μm. These microcracks grew slowly, emitting low-amplitude events, as the strain increased, but were prevented from causing failure at low strains because of the toughening effect of the glass fibers. At sufficiently high strains, however, fiber breakage and fiber pull-out occurred that corresponded to the high-amplitude events detected by the AE. At strains just prior to failure, catastrophic crack growth occurred, producing a rapid increase in both low-and high-amplitude events, causing ultimate failure.     

Effects of organo‐montmorillonite on the mechanical and morphological properties of epoxy/glass fiber composites

Epoxy composites filled with glass fiber and organo‐montmorillonite (OMMT) were prepared by the hand lay‐up method. The flexural properties of the epoxy/glass fiber/OMMT composites were characterized by a three‐point bending test. The flexural modulus and strength of epoxy/glass fiber were increased significantly in the presence of OMMT. The optimum loading of OMMT in the epoxy/glass fiber composites was attained at 3 wt%, where the improvement in flexural modulus and strength was approximately 66 and 95%, respectively. The fractured surface morphology of the epoxy/glass fiber/OMMT composites was investigated using field emission scanning electron microscopy. It was found that OMMT adheres on the epoxy/glass fiber interface, and this is also supported by evidence from energy dispersive X‐ray analysis. Copyright © 2007 Society of Chemical Industry     

Atomic oxygen effects on the prefailure damage processes in highly filled glass/mica/epoxy composites

In the present study, the effect of atomic oxygen (AO) exposure, as a simulation of low earth orbit, on the flexural properties and prefailure damage mechanisms of a series of short glass fiber/mica/epoxy composites under three-point bending were elucidated using acoustic emission (AE) techniques. The incorporation of mica in the composites was shown to increase the resistance to AO as measured by the weight loss, ashing rate, and reaction efficiency. Furthermore, as the mica content increased, the resistance increased such that the all-mica composite had over one order of magnitude lower ashing rate and reaction efficiency than did the all-glass-fiber composite. This increased resistance was caused by the mica particles preferentially orienting parallel to the surface of the composites, creating an inorganic barrier to attack. The AO-induced erosion was found to have an insignificant effect on both the flexural properties and prefailure damage mechanisms because the erosion was confined to the epoxy surface only and did not affect the bulk.     

Effect of coupling agents on thermal and electrical properties of mica/epoxy composites

The influence of 3-aminopropyltriethoxysilane, 3-glycidyloxypropyltrimethoxysilane, and neoalkoxytric(dioctyl pyrophosphato)zirconate on thermal expansion behavior, dielectric strength, and arc resistance of mica/epoxy composites has been investigated. The addition of mica up to 30% resulted in the reduction of thermal expansion with respect to neat resin. However, the coefficient of linear thermal expansion of 30% mica treated with aminosilane was the least among the various coupling agent-coated filler/epoxy composites. Mica (30%)/epoxy composites showed the highest dielectric strength values (26 kV/mm), but the highest arc resistance was obtained in zirconate-treated mica (30%)/epoxy composite. © 1995 John Wiley & Sons, Inc.     

Mica reinforced nylon‐6: Effect of coupling agents on mechanical,thermal, and dielectric properties

The effects of applying titanate (TYZOR® TPT) and silane (DYNASYLAN VTMO) coupling agents to wet ground muscovite mica in nylon‐6 composites are described. Nylon‐6 composites of 5–40 wt % filler loadings were compounded using an APV Baker twin‐screw extruder. Mica (25 wt %) brought about an increase in the Young's modulus, flexural strength, and flexural modulus but did not produce significant variations in tensile and impact strength. Hence different coupling agents were employed. It was observed that titanate coupling agent improved the tensile strength and the Young's modulus of the composites much while the impact properties were enhanced by the silane coupling agent. An attempt was made to use ?‐caprolactum in improving the interfacial adhesion of the filler and the matrix. It was observed that ?‐caprolactum improved the flexural modulus of the composites most. The effect of coupling agents on the dielectric strength, heat distortion temperature, and morphology were also investigated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4074–4081, 2006     

Flexural and Charpy impact behaviour of epoxy/glass fabric treated by nano-SiO2 and silane blend

A sizing formulation, containing compatible and incompatible silane coupling agents with epoxy resin in conjunction with nanoscale colloidal silica, was used to modify the surface of glass fabric. The modified glass fabric/epoxy resin composite panels were fabricated and characterised by flexural test, Charpy impact test and scanning electron microscope (SEM). By combining nano silica with silane blend in the fabric sizing, more energy was consumed under bending and impacting, which resulted in an improvement of the toughness in composites. The flexural strength, bending stain and Charpy impact strength of the epoxy composite/glass fabric treated with 1?wt-% nano silica and silane blend were ～42, ～22 and 35%, respectively, higher than those of silane blend coated glass fabric-reinforced composites (without nano silica). Furthermore, the change of the brittle fracture of the composite into ductile fracture was investigated by SEM micrographs. A possible toughening mechanism was also proposed.     

碳纤维湿法缠绕用环氧树脂基体研究

以TDE-85树脂和AFG-90树脂为主体树脂,混合芳香胺为固化剂,研究了一种适合于碳纤维复合材料湿法缠绕成型的树脂配方。结果表明,该树脂的黏度低(＜550 mPa·s)、适用期长,其浇铸体具有优异的力学性能,其拉伸强度为107 MPa,拉伸模量为4．09 GPa,弯曲强度为161 MPa,弯曲模量为3．88 GPa,断裂伸长率超过6%。用其制备的T-700碳纤维缠绕复合材料界面粘接好,NOL环层间剪切强度达到66．8 MPa,拉伸强度达到2．44 GPa。     

Flexural properties of S‐2 glass and TR30S carbon fiber‐reinforced epoxy hybrid composites

A study on the flexural properties of hybrid composites reinforced by S‐2 glass and TR30S carbon fibers is presented in this article. Test specimens were made by the hand lay‐up process in an intraply configuration with varying numbers of glass/epoxy laminas substituted for carbon/epoxy laminas. These specimens were then tested in the three point bend configuration in accordance with ASTM D790‐07 at a span to depth ratio of 32. The failed specimens were examined under an optical microscope, and the results show that the dominant failure mode is at the compressive side. The flexural behavior was also simulated by finite element analysis (FEA). Based on the FEA results, the flexural modulus and flexural strength were calculated. Good agreement is found between the experiments and FEA. It is shown that flexural modulus decreases with increasing percentage of S‐2 glass fibers, positive hybrid effects exist by substituting carbon fibers for glass fibers, and applying a thin layer of S‐2 glass fiber‐reinforced polymer on the compressive surface yields the highest flexural strength. The modeling approach presented will pave a way to the effective design of hybrid composites. POLYM. COMPOS., © 2012 Society of Plastics Engineers     

Delamination mechanism of high‐voltage coil insulators made from mica flakes and thermosetting epoxy resin

To clarify the delamination mechanism of high‐voltage coil insulators made from mica flakes and epoxy resin due to static mechanical stress, the relationships between the shear strength of the insulator and the physical properties of the component materials were studied. The mechanism of their delamination was thought to be either a lack of epoxy resin between the mica flakes, interface failure between the mica flakes and the epoxy resin, or cleavage of the mica flakes. The first two mechanisms were discounted because the shear strength of the insulator was found to be independent of both the contact angle of the corresponding liquid epoxy resin on the mica flakes and the critical surface tension of the epoxy resin. Furthermore, the shear strength of the model insulator was improved by using an epoxy resin with a higher bending elastic modulus, implying that the delamination mechanism in this system is the cleavage of mica flakes. Therefore, the epoxy resin should have a high elastic modulus to ensure high delamination resistance, that is, the temperature to which the insulators are exposed should be lower than the glass transition temperature of the corresponding epoxy resin. Optical microscope studies also supported these results. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 79: 2164–2169, 2001     

聚丙烯/马来酸酐接枝聚丙烯/环氧树脂/玻璃纤维复合材料的制备及其性能研究

通过双螺杆挤出机制备了聚丙烯/马来酸酐接枝聚丙烯/环氧树脂/玻璃纤维（PP/PP-g-MAH/EP/GF）复合材料,并研究了PP-g-MAH含量、EP含量及固化剂对复合材料力学性能的影响。结果表明,PP-g-MAH含量为10份,含有固化剂EP的含量为3份时,复合材料的综合力学性能最佳;与不加EP的复合材料相比,其拉伸强度、弯曲强度、冲击强度分别提高了41 %、47 %、86 %。扫描电子显微镜分析表明,EP的加入明显改善了GF和PP基体的黏结强度。     

Short glass fiber reinforced ABS and ABS/PA6 composites: Processing and characterization

In this study acrylonitrile‐butadiene‐styrene (ABS) terpolymer was reinforced with 3‐aminopropyltrimethoxysilane (APS)‐treated short glass fibers (SGFs). The effects of SGF concentration and extrusion process conditions, such as the screw speed and barrel temperature profile, on the mechanical properties of the composites were examined. Increasing the SGF concentration in the ABS matrix from 10 wt% to 30 wt% resulted in improved tensile strength, tensile modulus and flexural modulus, but drastically lowered the strain‐at‐break and the impact strength. The average fiber length decreased when the concentration of glass fibers increased. The increase in screw speed decreased the average fiber length, and therefore the tensile strength, tensile modulus, flexural modulus, and impact strength were affected negatively and the strain‐at‐break was affected positively. The increase in extrusion temperature decreased the fiber length degradation, and therefore the tensile strength, tensile modulus, flexural modulus, and impact strength increased. At higher temperatures the ABS matrix degraded and the mechanical strength of the composites decreased. To obtain a strong interaction at the interface, polyamide‐6 (PA6) at varying concentrations was introduced into the ABS/30 wt% SGF composite. The incorporation and increasing amount of PA6 in the composites broadened the fiber length distribution (FLD) owing to the low melt viscosity of PA6. Tensile strength, tensile modulus, flexural modulus, and impact strength values increased with an increase in the PA6 content of the ABS/PA6/SGF systems due to the improved adhesion at the interface, which was confirmed by the ratio of tensile strength to flexural strength as an adhesion parameter. These results were also supported by scanning electron micrographs of the ABS/PA6/SGF composites, which exhibited an improved adhesion between the SGFs and the ABS/PA6 matrix. POLYM. COMPOS. 26:745–755, 2005. © 2005 Society of Plastics Engineers     

Synthesis and characterization of chlorinated soy oil based epoxy resin/glass fiber composites

Composites with good toughness properties were prepared from chemically modified soy epoxy resin and glass fiber without additional petroleum based toughening agent. Chlorinated soy epoxy (CSE) resin was prepared from soybean oil. The CSE was characterised by spectral, and titration method. The prepared CSE was blended with commercial epoxy resin in different ratios and cured at 85°C for 3 h, and post cured at 225°C for 2 h using m‐phenylene diamine (MPDA) as curing agent. The cure temperatures of epoxy/CSE/MPDA with different compositions were found to be in the range of (151.2–187.5°C). The composite laminates were fabricated using epoxy /CSE/MPDA‐glass fiber at different compositions. The mechanical properties such as tensile strength (248–299 MPa), tensile modulus (2.4–3.4 GPa), flexural strength (346–379 MPa), flexural modulus (6.3–7.8 GPa) and impact strength (29.7–34.2) were determined. The impact strength increased with the increase in the CSE content. The interlaminor fracture toughness (G_IC) values also increased from 0.6953 KJ/m² for neat epoxy resin to 0.9514 KJ/m² for 15%CSE epoxy‐modified system. Thermogravimetric studies reveal that the thermal stability of the neat epoxy resin was decreased by incorporation of CSE. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Effects of chemical surface pretreatment on tensile properties of a single glass fiber and the glass fiber reinforced epoxy composite

The aim of this article is to determine the effect of surface pretreatments, prior to the silanization, on the structure and tensile properties of the glass fibers and their epoxy composites. Commercial glass fibers were washed with acetone to remove the soluble portion of sizing, calcinated for the removal of organic matter, activated for surface silanol regeneration, and silanizated with glycidoxypropyltrimethoxysilane (GPS). Tensile test was carried out. The morphology of pretreated glass fibers and the fracture surfaces of the epoxy composites were observed with a scanning electron microscope (SEM). The results revealed that both apparent modulus and strength of a single glass fiber and the glass fiber/epoxy resin composites strongly depend on the fiber surface pretreatments. The acetone treatment did not change appreciably the composition and tensile properties of glass fibers, but there was a weak interface between fibers and matrix. In calcinated and acid activated fibers, the two competitive effects was observed: (1) degradation of the fibers themselves and (2) improved interfacial adhesion between the glass fibers and the epoxy matrix, once the samples was silanizated. The ATR‐FTIR results show that the surface content of Si OH increases as reflected by the increasing of the Si O band, resulting in an interaction between silane coupling agent and glass fiber. POLYM. COMPOS., 91–100, 2016. © 2014 Society of Plastics Engineers     

环氧树脂/石英纤维透波复合材料制备

为改善环氧树脂的介电性能及提升石英纤维的界面性能,使用缩水甘油醚基笼型倍半硅氧烷(G–POSS)和γ–氨丙基三乙氧基硅烷(KH–550)分别对环氧树脂和石英纤维进行改性。利用差示扫描量热法研究改性后环氧树脂的固化过程,并通过外推法确定了其固化工艺,根据固化工艺制备环氧树脂/石英纤维复合材料,分别对该复合材料的热稳定性、介电性能和弯曲性能进行表征,结果表明,使用G–POSS和KH–550改性后的环氧树脂/石英纤维复合材料热稳定性、介电性能和弯曲性能达到最佳,初始分解温度达到369.59℃,常温下在12~18 GHz的介电常数稳定在3.2~3.5之间,介电损耗角正切值在0.005~0.02之间,弯曲强度达到376.4 MPa,弯曲弹性模量为21.7 GPa。     

Mechanical and Damping Properties of Glass Fiber and Mica-Reinforced Epoxy Composites

Mica/glass fiber-reinforced epoxy with 0° and 45° ply angle were prepared by hand lay-up and the mechanical and damping properties were studied. Results show that the addition of mica resulted in decrease of tensile strength and modulus for both composites. Althogh flexural strength and modulus of composites with 45° appeared a maximum at 5 phr mica loading, that of composites with 0° reached a maximum at 10 phr mica loading. For composites with 0°, damping ratio reaches maximum at 5 phr mica. Although for composites with 45°, damping ratio decrease with increasing mica loading.     

Improvement of Tensile and Flexural Properties in Epoxy/Clay Nanocomposites Reinforced with Weave Glass Fiber Reel

The tensile strength, tensile modulus, flexural strength and flexural modulus properties were investigated on epoxy/clay nanocomposites to assess the influence of nanoclay. Mechanical properties were significantly increased due to an increase in clay content up to 5 wt%, and decreased with a further increase in clay content. Optimal improvement of properties was observed with increased clay content up to 5 wt%. Duo properties of the glass fiber were improved by clay addition due to the improved interface between the glass fiber and epoxy. SEM analysis was conducted on different fractured surfaces to study the mechanical behavior.     

Flexibility improvement of short glass fiber reinforced epoxy by using a liquid elastomer

In certain applications of fiber reinforced polymer composites flexibility is required. The aim of this study was to improve flexibility of short glass fiber reinforced epoxy composites by using a liquid elastomer. For this purpose, diglycidyl ether of bisphenol-A (DGEBA) based epoxy matrix was modified with hydroxyl terminated polybutadiene (HTPB). A silane coupling agent (SCA) was also used to improve the interfacial adhesion between glass fibers and epoxy matrix. During specimen preparation, hardener and HTPB were premixed and left at room temperature for an hour before mixing with epoxy resin to allow possible reactions to occur. In order to compare flexibility of the specimens flexural tests were conducted and the data were evaluated numerically by using a derived relation. Test data and scanning electron microscope analysis indicated that surface treatment of glass fibers with SCA, and HTPB modification of epoxy matrix improved flexural properties especially due to the strong interaction between fibers, epoxy, and rubber. It was also observed that HTPB modification resulted in formation of relatively round rubber domains in the epoxy matrix leading to increased flexibility of the specimens.     

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.     

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     

Fabrication and characterization of functionally graded nanoclay/glass fiber/epoxy hybrid nanocomposite laminates

In this work, hardness, tensile, impact, bearing strength and water absorption tests were performed to study the mechanical properties of stepwise graded and non-graded hybrid nanocomposites. Three different stepwise graded nanocomposites and one non-graded (homogeneous) nanocomposite with the same geometry and total nanoclay content of 10 wt% were designed and prepared. Moreover, one neat glass fiber laminate was manufactured. The results of the tests indicated that addition of the graded and non-graded nanoclay improves hardness over neat glass fiber reinforcement. The maximum increase in hardness of about 53% over neat specimen is obtained for specimens that have the highest weight percentage (2 wt%) of the clay nanoparticles on its surface (S-specimen and the side of F-specimen that reinforced with 2 wt% nanoclay). The gradation process results in an increase in hardness of about 11% compared with non-graded (homogeneous) specimen. In addition, an improvement of 11.9% in strain-to-failure is achieved with specimen having greatest amount of nanoclay in the middle over neat glass fiber/epoxy composite. The other nanoclay-filled glass fiber composites have strain-to-failure close to neat glass fiber/epoxy. The addition of nanoclay reinforcement has insignificant effect on ultimate tensile strength, tensile modulus, water absorption, bearing strength and impact strength compared with neat glass fiber/epoxy.