Adhesion improvement in glass fiber reinforced polyethylene composite via admicellar polymerization

Admicellar polymerization (polymerization of monomer solubilized in adsorbed surfactant bilayers) has been used to form a thin film of polyethylene onto the surface of milled glass fibers using sodium dodecyl sulfate as the surfactant. The decrease in ethylene pressure was used to follow the solubilization and adsolubilization processes as well as the reaction processes. An increase in initiator (Na₂S₂O₈) to surfactant ratio gave thicker and more uniform coatings of polymer onto the glass fiber surface according to SEM micrographs. Although a substantial amount of ethylene polymerized in solution according to the pressure drop, the decrease in pressure attributed to admicelle polymerization corresponded to the amount of polymer formed on the glass fiber, indicating little, if any, solution polymer deposited on the fibers. The admicellar‐treated glass fiber was used to make composites with high‐density polyethylene. The composites showed an increase in tensile and flexural strength over composites made from as‐received glass fiber, indicating an improvement in the fiber‐matrix adhesion of the admicellar‐treated glass fiber.     

Studies on surface energetics of glass fabrics in an unsaturated polyester matrix system: Effect of sizing treatment on glass fabrics

The surfaces of glass fibers were sized by polyvinyl alcohol (PVA), polyester, and epoxy resin types in order to improve the mechanical interfacial properties of fibers in the unsaturated polyester matrix. The surface energetics of the glass fibers sized were investigated in terms of contact angle measurements using the wicking method based on the Washburn equation, with deionized water and diiodomethane as the wetting liquids. In addition, the mechanical behaviors of the composites were studied in the context of the interlaminar shear strength (ILSS), critical stress intensity factor (K_IC), and flexural measurements. Different evolutions of the London dispersive and specific (or polar) components of the surface free energy of glass fibers were observed after different sizing treatments. The experimental result of the total surface free energies calculated from the sum of their two components showed the highest value in the epoxy‐sized glass fibers. From the measurements of mechanical properties of composites, it was observed that the sizing treatment on fibers could improve the fiber–matrix interfacial adhesion, resulting in improved final mechanical behaviors, a result of the effect of the enhanced total surface free energy of glass fibers in a composite system. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1439–1445, 2001     

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     

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.     

原位聚合连续纤维增强聚甲基丙烯酸甲酯复合材料的界面及性能研究

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

Ionic interphase of glass fiber/polyamide 6,6 composites

Interfacial polymerization to polyamide 6, 6 followed by introduction of ionic groups was performed on the surface of short glass fibers. The ionic interphase-modified fibers were used with poly(ethylene-co-methacrylic acid) (DuPont Surlyn) to prepare composites with specific fiber-matrix interactions. Fiber treatment increased composite tensile and bending properties. An increase in the average fiber length was observed, which was attributed to a decrease in the fiber attrition during mixing. The effect of increasing temperature on the composite mechanical properties was studied. Different behavior was observed before and after the glass transition temperature, T_g, of the matrix. The dynamic mechanical measurements showed an increase in the T_g of the matrix after the treatments, which is attributed to a decrease in chain mobility at the interface resulting from increased interactions of the treated fiber surface with the polymer. Scanning electron microscopy of fractured composites after tensile tests revealed a smooth fiber surface with no polymer at the surface for the untreated composites. Adhered polymer was clearly observed on the surface of treated fibers, indicating better fiber wetting by the matrix. This improved adhesion was attributed to the grafted nylon molecules at the glass fiber surface.     

Polymerization compounding composites of nylon‐6,6/short glass fiber

Nylon‐6,6 was grafted onto the surface of short glass fibers through the sequential reaction of adipoyl chloride and hexamethylenediamine onto the fiber surface. Grafted and unsized short glass fibers (USGF) were used to prepare composites with nylon‐6,6 via melt blending. The glass fibers were found to act as nucleating agents for the nylon‐6,6 matrix. Grafted glass fiber composites have higher crystallization temperatures than USGF composites, indicating that grafted nylon‐6,6 molecules further increase crystallization rate of composites. Grafted glass fiber composites were also found to have higher tensile strength, tensile modulus, dynamic storage modulus, and melt viscosity than USGF composites. Property enhancement is attributed to improved wetting and interactions between the nylon‐6,6 matrix and the modified surface of glass fibers, which is supported by scanning electron microscopy (SEM) analysis. The glass transition (tan δ) temperatures extracted from dynamic mechanical analysis (DMA) are found to be unchanged for USGF, while in the case of grafted glass fiber, tan δ increases with increasing glass fiber contents. Moreover, the peak values (i.e., intensity) of tan δ are slightly lower for grafted glass fiber composites than for USGF composites, further indicating improved interactions between the grafted glass fibers and nylon‐6,6 matrix. The Halpin‐Tsai and modified Kelly‐Tyson models were used to predict the tensile modulus and tensile strength, respectively.     

Polyester composites reinforced with noncrimp stitched glass fabrics: Experimental characterization of composites and investigation on the interaction between glass fiber and polyester matrix

The primary purpose of the study was to investigate the anisotropic behavior of different noncrimp stitched fabric reinforced polyester composites. The effects of geometric variables on composite structural integrity and strength are illustrated. Hence, tensile, three‐point bending flexural and short beam shear tests were conducted up to failure on specimens strengthened with different layouts of fibrous plies in noncrimp stitched fabric. The remark, based on the observations while tensile testing, is that the stress–strain curves of polyester based composites were linear in the direction of fibers. However, in the matrix dominated orientations nonlinear relation between the stress and the strain was observed. Another aim of the present work was to investigate the interaction between glass fiber and polyester matrix. The experiments, in conjunction with scanning electron photomicrographs of fractured surfaces of composites, were interpreted in an attempt to explain the interaction between glass fiber and polyester and were interpreted in an attempt to explain the instability of polyester resin–glass fiber interfaces. It was concluded that the polymer was either deposited between adjacent fibers or as widely separated islands on the fiber surface. Infrared spectra of the cured polyester and its glass fiber composite were obtained by Fourier transform infrared spectroscopy. POLYM. COMPOS., 2008. © 2007 Society of Plastics Engineers     

Hybrid fiber fabric composites from poly ether ether ketone and glass fiber

Poly ether ether ketone (PEEK) polymer was extruded into filaments and cowoven into unidirectional hybrid fabric with glass as reinforcement fiber. The hybrid fabrics were then converted into laminates and their properties with special reference to crystallization behavior has been studied. The composite laminates have been evaluated for mechanical properties, such as tensile strength, interlaminar shear strength (ILSS), and flexural strength. The thermal behavior of the composite laminates were analyzed using differential scanning calorimeter, thermogravimetric analyzer, dynamic mechanical analyzer (DMA), and thermomechanical analyzer (TMA). The exposure of the fabricated composite laminates to high temperature (400 and 500°C) using radiant heat source resulted in an improvement in the crystallanity. The morphological behavior and PEEK resin distribution in the composite laminates were confirmed using scanning electron microscope (SEM) and nondestructive testing (NDT). Although DMA results showed a loss in modulus above glass transition temperature (T_g), a fair retention in properties was noticed up to 300°C. The ability of the composite laminates to undergo positive thermal expansion as confirmed through TMA suggests the potential application of glass–PEEK composites in aerospace sector. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci 117:1446–1459, 2010     

Concentration effect of γ‐glycidoxypropyltrimethoxysilane on the mechanical properties of glass fiber–epoxy composites

In this study, glass fibers were modified using γ‐glycidoxypropyltrimethoxysilane of different concentrations to improve the interfacial adhesion at interfaces between fibers and matrix. Effects of γ‐glycidoxypropyltrimethoxysilane on mechanical properties and fracture behavior of glass fiber/epoxy composites were investigated experimentally. Mechanical properties of the composites have been investigated by tensile tests, short beam tests, and flexural tests. The short‐beam method was used to measure the interlaminar shear strength (ILSS) of laminates. The tensile and flexural properties of composites were characterized by tensile and three‐point bending tests, respectively. The fracture surfaces of the composites were observed with a scanning electron microscope. On comparing the results obtained for the different concentrations of silane solution, it was found that the 0.5% GPS silane treatment provided the best mechanical properties. The ILSS value of heat‐cleaned glass fiber reinforced composite is enhanced by ∼59% as a result of the glass fiber treatment with 0.5% γ‐GPS. Also, an improvement of about 37% in tensile strength, about 78% in flexural strength of the composite with the 0.5% γ‐GPS treatment of glass fibers was observed. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Physical,mechanical, and water absorption behavior of coir/glass fiber reinforced epoxy based hybrid composites

Fiber reinforced polymer composites has been used in a variety of application because of their many advantages such as relatively low cost of production, easy to fabricate, and superior strength compare to neat polymer resins. Reinforcement in polymer is either synthetic or natural. Synthetic fiber such as glass, carbon, etc. has high specific strength but their fields of application are limited due to higher cost of production. Recently there is an increase interest in natural composites which are made by reinforcement of natural fiber. In this connection, an investigation has been carried out to make better utilization of coconut coir fiber for making value added products. The objective of the present research work is to study the physical, mechanical, and water absorption behavior of coir/glass fiber reinforced epoxy based hybrid composites. The effect of fiber loading and length on mechanical properties like tensile strength, flexural strength, and hardness of composites is studied. The experimental results reveal that the maximum strength properties is observed for the composite with 10 wt% fiber loading at 15 mm length. The maximum flexural strength of 63 MPa is observed for composites with 10 wt% fiber loading at 15 mm fiber length. Similarly, the maximum hardness value of 21.3 Hv is obtained for composites with 10 wt% fiber loading at 20 mm fiber length. Also, the surface morphology of fractured surfaces after tensile testing is examined using scanning electron microscope (SEM). POLYM. COMPOS., 35:925–930, 2014. © 2013 Society of Plastics Engineers     

玻纤增强玻璃复合材料抗弯和抗热震性能研究

采用"三明治"结构法将玻纤与硼硅酸盐玻璃基体复合成为玻纤增强玻璃复合材料,并对其抗弯性能以及抗热震性能进行了测试和分析。结果表明:在纤维体积分数为50%时,复合材料的抗弯强度较高,韧性更好;玻纤增强玻璃复合材料的抗热震性能相较于玻璃有显著地提高。     

Mechanical properties of glass/flax hybrid composites based on a novel modified soybean oil matrix material

In the Affordable Composites from Renewable Resources (ACRES) program at the University of Delaware, soybean oil and other plant triglycerides have been made amenable to polymerization using a broad range of chemical routes. The resultant polymers range in properties from soft rubbers to hard thermosets for composite applications. In this paper we present an investigation of the mechanical properties of glass/flax hybrid composites based on these thermoset matrix materials. Composites with different glass/flax ratios and different fiber arrangements were made using a modified soybean oil matrix material. The fiber arrangement was varied to make symmetric and unsymmetric composites. The latter were tested in different modes in flexural tests and drop weight impact tests. The mechanical properties of the composites were found to depend upon the glass/flax ratio and the arrangement of fibers in the composite. On proper selection of the arrangement of fibers in the composite, the glass fibers and flax fibers were found to act synergistically resulting in an improved flexural and impact performance. POLYM. COMPOS., 26:407–416, 2005. © 2005 Society of Plastics Engineers     

Static and dynamic mechanical properties of a kenaf fiber–wood flour/polypropylene hybrid composite

A natural fiber hybrid composite containing equal proportions of kenaf fibers (KFs) and wood flour (WF) as the reinforcements and polypropylene (PP) as the polymer matrix was prepared, and its static and dynamic mechanical properties were compared with KF/PP and WF/PP composites. Static tensile and flexural tests and dynamic mechanical analysis (DMA) were carried out. The hybrid composite exhibited tensile and flexural moduli and strength values closer to those of the KF composite, which indicated a higher reinforcing efficiency of KFs compared with WF. DMA revealed that although the glass‐transition temperature remained unchanged by the replacement of half of the WF by KFs, the α‐transition temperature of the hybrid composite was identical to that of WF composite. The magnitudes of both the α and β (glass) transitions of the hybrid composite were comparable to that of the WF/PP composite. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 665–672, 2005     

Injection‐molded short hemp fiber/glass fiber‐reinforced polypropylene hybrid composites—Mechanical,water absorption and thermal properties

Natural fiber‐based thermoplastic composites are generally lower in strength performance compared to thermoset composites. However, they have the advantage of design flexibility and recycling possibilities. Hybridization with small amounts of synthetic fibers makes these natural fiber composites more suitable for technical applications such as automotive interior parts. Hemp fiber is one of the important lignocellulosic bast fiber and has been used as reinforcement for industrial applications. This study focused on the performance of injection‐molded short hemp fiber and hemp/glass fiber hybrid polypropylene composites. Results showed that hybridization with glass fiber enhanced the performance properties. A value of 101 MPa for flexural strength and 5.5 GPa for the flexural modulus is achieved from a hybrid composite containing 25 wt % of hemp and 15 wt % of glass. Notched Izod impact strength of the hybrid composites exhibited great enhancement (34%). Analysis of fiber length distribution in the composite and fracture surface was performed to study the fiber breakage and fracture mechanism. Thermal properties and resistance to water absorption properties of the hemp fiber composites were improved by hybridization with glass fibers. Overall studies indicated that the short hemp/glass fiber hybrid polypropylene composites are promising candidates for structural applications where high stiffness and thermal resistance is required. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2432–2441, 2007     

Mechanical properties of glass fabric/polyester composites: Effect of silicone coatings on the fabrics

An experimental investigation was carried out to study the effect of a silicone coating on the mechanical properties of polyester/woven glass fabric composites, fabricated by resin transfer molding. E‐glass woven fabrics were coated with a silicone elastomer by solution dip coating. The effect of variation of silicone amounts on the impact resistance, toughness, and mechanical properties of the composite was determined. Short beam shear tests were performed to assess the effect of coating on the adhesion of the fiber to the matrix. The coated specimens exhibited worse interlaminar shear strength over that of uncoated fabrics. Three‐point bending tests were also performed to investigate the effect of the coating on flexural properties. Whereas flexural strength and Young's modulus decreased with increasing amount of coating, the toughness, represented by the area under the stress–strain curve, presented a maximum. Finally, notched Izod impact tests were carried out and the curve for the energy absorbed during impact versus the amount of coating also appeared to have a maximum, indicating an interesting slot for optimum impact performance. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 1300–1308, 2004     

Processing and properties of solution impregnated carbon fiber reinforced polyethersulfone composites

Carbon fiber reinforced polymer composites are attractive because of their high stiffness and strength‐to‐weight ratios. In order to fully utilize the stiffness and strength of the reinforcement fiber, it is necessary to bring the polymer matrix and the reinforcement fiber together with homogeneous wetting. In this paper, a solution processing technique and the mechanical properties of carbon fiber reinforced polyethersulfone composites were investigated. The polymer was dissolved in cyclopentanone and fed onto a continuous carbon fiber tow using a drum winder. The solution‐processed composite prepregs were then layed up and compression molded into unidirectional composite panels for evaluation. The composite samples showed uniform fiber distribution and reasonably good wetting. The longitudinal flexural modulus was as high as 137 GPa, and longitudinal flexural strength 1400 MPa. In addition, the effects of polymer grade and processing conditions on the mechanical properties of the composites were discussed. It is suggested that the transverse properties and interlaminar fracture toughness could benefit from higher polymer matrix molecular weight. A careful design in the spatial distribution of the molecular weight would be necessary for practical applications.     

Improved hydrothermal aging performance of glass fiber-reinforced polymer composites via silica nanoparticle coating

The long-term exposure to a hot and humid environment severely damages the bonding integrity of fiber-reinforced polymer composites and thus significantly degrades their mechanical performances. In this work, we aim to develop an improvement procedure for effectively enhancing the bonding strength in glass fiber-reinforced polymers (GFRPs). Glass fibers were coated with a thin layer of silica nanoparticles of different concentrations by the use of the evaporative deposition method. Micromorphological comparisons in terms of scanning electron microscope imaging demonstrate significant improvements on the surface roughness of glass fibers. With the coated glass fibers, GFRP composite laminates were designed, molded through the vacuum-assisted resin infusion technique, and experimentally tested for quantitatively studying their hydrothermal aging performance. The water absorption tests conducted for three exposure temperatures suggest that both the water diffusion rate and the equilibrium water content can be effectively reduced due to the introduction of the silica coating. With increased exposure temperatures, however, the desired reductions become much less significant. A so-called water-channel diffusion mechanism along fiber/resin interfaces was proposed to explain the coupling effects of silica coating and exposure temperature. Reductions of water diffusion rate and equilibrium water content were expected to slow down the hydrothermal aging performance of GFRPs. For this purpose, both uniaxial tensile test and three-point bending test were subsequently performed on GFRP specimens that have been subjected to different coating concentrations, exposure temperatures, and exposure durations. When compared with untreated GFRP specimens, both experiments demonstrate that the residual strength and stiffness can be effectively promoted through coating a thin layer of silica nanoparticles on glass fiber surfaces. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48652.     

陶瓷基复合材料的界面相容性研究

有关陶瓷基复合材料（CMC）的界面问题已经得到广泛的重视。为了使材料达到一个很好的刚性，在纤维与基体之间保持尽量小的界面作用力对于陶瓷纤维增强Si-C-O复合材料是非常重要的。在纤维界面上涂层有利于减小它们之间相互作用，涂层处理后的Si-C-O复合材料的弯曲强度比一般无涂层的复合材料高5倍。在介质涂层、基体、以及涂层与纤维间的三相物质中避免化学反应的发生。目前，可利用化学相容性的原理对涂层纤维进行选择。     

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