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

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

Recycling studies of marble processing waste: Composites based on commercial epoxy resin

Marble waste was obtained from marble processing plant wastewater with precipitation using different coagulants, such as sepiolite, zeolite, and pumice in dosages of 0.5–8 g/500 mL and mixed in 20 wt % with commercial epoxy resin. The effects of marble, coagulant type and dosage on the physicomechanical and thermal properties were investigated. The incorporation of marble processing waste particles increases the 10% decomposition temperature of pure epoxy by 5–50°C. Surface hardness, tensile strength, percentage elongation, and stress at maximum load of the composites were higher than those of pure resin, too. The composites reinforced with marble processing waste-pumice showed about 10% increase in elastic modulus, whereas the composite reinforced with marble processing waste-sepiolite or zeolite showed about 76.67–143.33% increase in elastic modulus over the pure epoxy matrix. Scanning electron microscopy (SEM) was used for characterization of surface and cross sections of the composites to verify the results. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Unsaturated polyester‐toughened epoxy composites: Effect of sisal fiber on thermal and dynamic mechanical properties

In the present study, the mechanical and thermal properties of sisal fiber‐reinforced unsaturated polyester (UP)‐toughened epoxy composites were investigated. The sisal fibers were chemically treated with alkali (NaOH) and silane solutions in order to improve the interfacial interaction between fibers and matrix. The chemical composition of resins and fibers was identified by using Fourier‐transform infrared spectroscopy. The UP‐toughened epoxy blends were obtained by mixing UP (5, 10, and 15 wt%) into the epoxy resin. The fiber‐reinforced composites were prepared by incorporating sisal fibers (10, 20, and 30 wt%) within the optimized UP‐toughened epoxy blend. Scanning electron microscopy was used to analyze the morphological changes of the fibers and the adhesion between the fibers and the UP‐toughened epoxy system. The results showed that the tensile and flexural strength of (alkali‐silane)‐treated fiber (30 wt%) ‐reinforced composites increased by 83% and 55%, respectively, as compared with that of UP‐toughened epoxy blend. Moreover, thermogravimetric analysis revealed that the (alkali‐silane)‐treated fiber and its composite exhibited higher thermal stability than the untreated and alkali‐treated fiber systems. An increase in storage modulus and glass transition temperature was observed for the UP‐toughened epoxy matrix on reinforcement with treated fibers. The water uptake behavior of both alkali and alkali‐silane‐treated fiber‐reinforced composites is found to be less as compared with the untreated fiber‐reinforced composite. J. VINYL ADDIT. TECHNOL., 23:188–199, 2017. © 2015 Society of Plastics Engineers     

Synthesis and characterization of a new class of thermosetting resins: Allyl and propargyl substituted cyclopentadiene derivatives

A series of all-hydrocarbon resins were synthesized by reacting cyclopentadiene allyl chloride, propargyl chloride, or a mixture of allyl chloride and propargyl ide, under phase transfer conditions. Phase transfer reactions with and without added solvents, and with either quaternary ammonium or crown ether catalysts, yielded similar products consisting of a mixture of 1,1-disubstituted cyclopentadiene (minor amount) and 2-3 isomers each of tri-, tetra-, penta-, and hexa-substituted derivatives. No further reaction of each these components possible. The overall substitution pattern varied little with changes in reaction conditions although limiting the allyl chloride content led to still reactive, partially substituted products. Incorporation of all-propargyl and high propargyl-to-allyl mixed functionalities on cyclopentadiene yielded products whose stability was very hindering their thorough characterization. Preliminary evaluation was there-carried out for mixed resins with lower propargyl functionality. The allyl substituted resin (allylated cyclopentadiene, ACP) underwent thermal cure lout initiator at around 200°C while allyl/propargyl substituted resin (7:1 ratio, APCP) showed a faster, lower temperature cure at around 120°C. Cationic cure of ACP was also initiated by a novel sulfonium salt at around 100°C. Neat resin when cured at 200°C gave material with a flexural storage modulus 2 of about 300 MPa. Further cure at 250°C raised the modulus to 1.2 GPa. resin gave composites with excellent properties when used with glass and on fibers. Flexural modulus values (by DMA) of ∼ 66 GPa were obtained for ACP/carbon fiber composites compared with 42 GPa for epoxy/carbon composites made in our laboratories using commercially available materials. The modulus values at 300°C dropped to 10% of the room temperature value for the epoxy composites, while the ACP/carbon composite maintained 60% of its room temperature value at 300°C. When brought back to ambient temperature, the modulus of latter sample had increased to 80 GPa and that of the epoxy composite dropped to 23 GPa. Glass fiber ACP composites performed similar to an epoxy composite up to 200°C but maintained properties up to 300°C while those of the epoxy were drastically reduced. TGA analysis of both cured ACP resin and its composites showed decomposition beginning at 375°C. Three-point-bending tests indicated very high modulus with brittle failure for ACP composites. Scanning electron micrographs showed moderate bonding of the new resin to both carbon glass fiber surfaces. This new class of thermosetting resins offers excellent potential for application in low-cost glass and carbon composites with good thermal and physical properties.     

Recycled polypropylene reinforced with curaua fibers by extrusion

Curaua fibers were studied as reinforcing agents for postconsumer polypropylene. The composites were processed by extrusion. The composite properties were investigated by mechanical tests, thermal methods, melt flow index, surface morphology, and water uptake. The variables studied were as follows: fiber contents (10 to 40 wt %), fiber surface treatment, initial fiber length, and modification of the polypropylene matrix. The treatment of the fiber with 5 wt % NaOH aqueous solution did not improve fiber‐matrix adhesion and the composites using 20 wt % of untreated curaua fibers presented the better mechanical properties. Feeding the extruder with fibers having shorter lengths (0.01–0.4 mm) produced better fiber dispersion, improving the mechanical properties of the composites. Composites prepared using fibers without surface treatment with postconsumer polypropylene and with polypropylene modified with maleic anhydride showed mechanical properties and water uptake similar to composites using the same polymer reinforced with other lignocellulosic fibers. The extrusion process caused also partial fibrillation of the fibers, improving their aspect ratio. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of the talc filler content on the mechanical properties of polypropylene composites

This research examines the effect of a microsize/nanosize talc filler on the physicochemical and mechanical properties of filled polypropylene (108MF10 and 33MBTU from Saudi Basic Industries Corp. and HE125MO grade from Borealis) composite matrices. A range of mechanical properties were measured [tensile properties, bending properties, fracture toughness, notched impact strength (at the ambient temperature and ?20°C), strain at break, and impact strength] along with microhardness testing and thermal stability testing from 40 to 600°C as measured by differential thermal analysis and thermogravimetric analysis. Increasing filler content lead to an increase in the mechanical strength of the composite material with a simultaneous decrease in the fracture toughness. The observed increase in tensile strength ranged from 15 to 25% (the maximum tensile strength at break was found to be 22 MPa). The increase in mechanical strength simultaneously led to a higher brittleness, which was reflected in a decrease in the mean impact strength from the initial 18 kJ/m² (for the virgin polypropylene sample) to 14 kJ/m², that is, a 23% decrease. A similar dependency was also obtained for the samples conditioned at ?20°C (a decrease of 12.5%). With increasing degree of filling of the talc–polypropylene composite matrix, the thermooxidative stability increased; the highest magnitude was obtained for the 20 wt % sample (decomposition temperature = 482°C, cf. 392°C for the virgin polymer). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Comparative study of interphase evolution in polysiloxane resin-derived matrix containing carbon micro and nanofibers during thermal treatment

The work presents the results of research on composite materials made of silicon-containing polymer-derived ceramic matrix composites (PDC-Cs) and nanocomposites (PDC-NCs). Carbon micro and nanofibers (CFs and CNFs) were used as reinforcements. The interactions between carbon micro and nanofibers and polysiloxane matrix, as well as interphase evolution mechanism in composite samples during their heating to 1000 °C were studied. CF/resin and CNF/resin composites were prepared via liquid precursor infiltration process of unidirectionally aligned fibers. After heating to 700 °C–800 °C, decomposition of the resin in the presence of CNFs led to the formation of fiber/organic-inorganic composites with pseudo-plastic properties and improved oxidation resistance compared to as-prepared fiber/resin composites. The most favourable mechanical properties and oxidation resistance were obtained for composites and nanocomposites containing the maximum amount of carbon nanoparticles precipitated in the SiOC matrix during the heat treatment at 800 °C. The precipitated carbon phase improves fiber/matrix adhesion of composites.     

Development of a bio‐based composite material from soybean oil and keratin fibers

A novel bio‐based composite material, suitable for electronic as well as automotive and aeronautical applications, was developed from soybean oils and keratin feather fibers (KF). This environmentally friendly, low‐cost composite can be a substitute for petroleum‐based composite materials. Keratin fibers are a hollow, light, and tough material and are compatible with several soybean (S) resins, such as acrylated epoxidized soybean oil (AESO). The new KFS lightweight composites have a density ρ ≈ 1 g/cm³, when the KF volume fraction is 30%. The hollow keratin fibers were not filled by resin infusion and the composite retained a significant volume of air in the hollow structure of the fibers. Due to the retained air, the dielectric constant, k, of the composite material was in the range of 1.7–2.7, depending on the fiber volume fraction, and these values are significantly lower than the conventional silicon dioxide or epoxy, or polymer dielectric insulators. The coefficient of thermal expansion (CTE) of the 30 wt % composite was 67.4 ppm/°C; this value is low enough for electronic application and similar to the value of silicon materials or polyimides used in printed circuit boards. The water absorption of the AESO polymer was 0.5 wt % at equilibrium and the diffusion coefficient in the KFS composites was dependent on the keratin fiber content. The incorporation of keratin fibers in the soy oil polymer enhanced the mechanical properties such as storage modulus, fracture toughness, and flexural properties, ca. 100% increase at 30 vol %. The fracture energy of a single keratin fiber in the composite was determined to be about 3 kJ/m² with a fracture stress of about 100–200 MPa. Considerable improvements in the KFS composite properties should be possible by optimization of the resin structure and fiber selection. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 95: 1524–1538, 2005     

Synthesis,morphology and physical properties of multi-walled carbon nanotube/biphenyl liquid crystalline epoxy composites

We have developed multi-walled carbon nanotube/liquid crystalline epoxy composites and studied the effects of incorporation carbon nanotubes (CNTs) on the morphology, thermal and mechanical properties of the composites. The CNTs are functionalized by liquid crystalline (LC) 4,4′-bis(2,3-epoxypropoxy) biphenyl (BP) epoxy resin for the ease of dispersion and the formation of long range ordered structure. The epoxy functionalized CNT (ef-CNT) were dispersed in the LC BP epoxy resin that can be thermal cured with an equivalent of 4,4′-diamino-diphenylsulfone to form composite. The curing process was monitored by polarized optical microscopy. The results indicate the LC resin was aligned along the CNTs to form fiber with dendritic structure initially then further on to obtain micro-sized spherical crystalline along with fibrous crystalline. With homogeneous dispersion and strong interaction between nanotubes and matrix, the composite containing 2.00 wt.% ef-CNT exhibits excellent thermal and mechanical properties. When the amount of ef-CNT exceeds 2.00 wt.%, vitrification stage of curing is fast reached, which lowers the degree of conversion. As compared with the neat resin, the composite containing 2.00 wt.% ef-CNT increases the glass transition temperature by 70.0 °C, the decomposition temperature by 13.8 °C, the storage modulus by 40.9%, and the microhardness by 63.3%.     

Effect of zeolite filler on the thermal degradation kinetics of polypropylene

In this study, the thermal degradation behavior of polypropylene (PP) and PP–zeolite composites was investigated. Clinoptilolite, a natural zeolitic tuff, was used as the filler material in composites. The effects of both pure clinoptilolite and silver‐ion‐exchanged clinoptilolite on the thermal degradation kinetics of the PP composites was studied with differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Polymer degradation was evaluated with DSC at heating rates of 5, 10, and 20°C/min from room temperature to 500°C. The silver concentration (4.36, 27.85, and 183.8 mg of Ag/g of zeolite) was the selected parameter under consideration. From the DSC curves, we observed that the heat of degradation values of the composites containing 2–6% silver‐exchanged zeolite (321–390 kJ/kg) were larger than that of the pure PP (258 kJ/kg). From the DSC results, we confirmed that the PP–zeolite composites can be used at higher temperatures than the pure PP polymer because of its higher thermal stability. The thermal decomposition activation energies of the composites were calculated with both the Kissinger and Ozawa models. The values predicted from these two equations were in close agreement. From the TGA curves, we found that zeolite addition into the PP matrix slowed the decomposition reaction; however, silver‐exchanged zeolite addition into the matrix accelerated the reaction. The higher the silver concentration was, the lower were the thermal decomposition activation energies we obtained. As a result, PP was much more susceptible to thermal decomposition in the presence of silver‐exchanged zeolite. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 143–148, 2006     

纳米玻璃粉掺杂双酚A型环氧树脂基复合材料的热稳定性能研究

采用双酚A型环氧树脂为基体,短切玻璃纤维和纳米玻璃粉为填料,通过模压加工工艺制备了双酚A型环氧树脂基复合材料。使用热失重分析仪和扫描电子显微镜分析研究了纳米玻璃粉含量对复合材料热稳定性能的影响,同时利用Kissinger法和Flynn?Wall?Ozawa法求解了双酚A型环氧树脂基复合材料的热分解动力学参数。结果表明,添加短切玻璃纤维后,双酚A型环氧树脂的最大热分解温度从365 ℃提高至369 ℃,而随着纳米玻璃粉的加入,其最大热分解温度进一步提升5 ~16 ℃。且复合材料的残炭率在65.41 %~69.15 %之间,相比双酚A型环氧树脂、短切玻璃纤维增强双酚A型环氧树脂基复合材料分别提高了69.88 %~71.51 %、22.95 %~27.11 %。同时纳米玻璃粉的加入也使得复合材料的热分解活化能得到提升,最高为153.14 kJ/mol,相比双酚A型环氧树脂单体及短切玻璃纤维材料增强双酚A型环氧树脂基复合材料的热分解活化能135.65 kJ/mol、137.46 kJ/mol显著增加。结果表明,纳米玻璃粉的引入改变了双酚A型环氧树脂基复合材料的内部微观结构,从而提高了其热稳定性能。     

Optimal performances of ultrasound treated kenaf fiber reinforced recycled polypropylene composites as demonstrated by response surface method

Kenaf fiber (KF) reinforced recycled polypropylene (RPP) composites were produced by melt cast method. To improve interfacial adhesion between fiber and RPP matrix, fiber surface modification was carried out by means of ultrasound treatment. Maleic anhydride grafted polypropylene (MAPP) was used as a coupling agent. Composites were examined by mechanical test, melt flow indexing test, scanning electron microscopy, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). Water uptake analysis and accelerated weathering test were carried out to find the suitability of the composites in outdoor application. Among the raw fiber contents ranging 10?50 wt % in the composites, the maximum tensile strength (TS) was observed at 40 wt % KF loading without using MAPP. Treated KF‐based composite with MAPP promotes this maximum TS value, which is 57% higher than that of raw KF‐based composite. TGA and DSC analyses exhibit an enhancement of thermal stability in treated KF‐reinforced RPP composites with MAPP. Incorporation of MAPP in the composites shows higher activation energy, suggesting improved interfacial bonding between fibers and matrix. Response surface method was employed to demonstrate the optimal treatment parameters for TS, showing excellent agreement with the observed values. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Experimental study on dielectric relaxation in alfa fiber reinforced epoxy composites

Investigation on dielectric properties and behavior of thermoset epoxy composite based on cellulosic fibers has been carried on. Dielectric spectra were measured in the frequency range 0.1 Hz–100 kHz and at temperature intervals from ambient to 200°C. For the composite, four relaxations processes were identified, namely the orientation polarization imputed to the presence of polar water molecules in Alfa fiber, the α mode relaxation associated with the glass transition of the epoxy resin matrix, the relaxation process associated with conductivity occurring as a result the carriers charges diffusion noted for high temperature above glass transition and low frequencies, and interfacial or Maxwell‐Wagner‐Sillars relaxation that is attributable to the accumulation of charges at the Alfa fibers/epoxy resin interfaces. Dielectric relaxation analysis revealed evolution in water relaxation and it is thus concluded that the chemical treatment of the fiber can strongly influence the dielectrical properties and interfacial polarization processes in composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Polypropylene–nanosilica‐filled composites: Effects of epoxy‐resin‐grafted nanosilica on the structural,thermal, and dynamic mechanical properties

This article reports a comparative study of polypropylene (PP) nanocomposites synthesized with nanosilica (NS) and diglycidyl ether of bisphenol A, an epoxy‐resin‐grafted nanosilica (ENS), as nanofillers. These nanocomposites were prepared with the melt‐mixing method at a constant loading level of 2.5 wt %; this loading level was much lower than that used for fillers in conventional composites. The effects of pure NS and ENS on the thermal, structural, mechanical, and dynamic mechanical properties of PP were analyzed with wide‐angle X‐ray diffraction, transmission electron microscopy, thermogravimetric analysis, differential scanning calorimetry, dynamic mechanical analysis, and scanning electron microscopy. The transmission electron microscopy studies showed a better dispersion of ENS in the PP matrix, that is, in the polypropylene‐epoxy‐resin‐grafted nanosilica (PP–ENS) nanocomposite, in comparison with NS in the PP matrix, that is, in the polypropylene–nanosilica (PP–NS) nanocomposite. Also, the thermogravimetric analysis results showed a higher thermal stability for PP–ENS than PP–NS. Furthermore, the dynamic mechanical analysis studies showed an increase in the elastic modulus and glass‐transition temperature for PP–ENS with respect to PP–NS. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2117–2124, 2006     

FTIR and SEM analysis of polyester‐ and epoxy‐based composites manufactured by VARTM process

Polyester‐ and epoxy‐based composites containing glass and carbon fibers were manufactured using a vacuum‐assisted resin transfer molding (VARTM) process. Fourier transform infrared (FTIR) spectroscopy analyses were conducted to determine the interaction between fibers and matrix material. The results indicate that strong interaction was observed between carbon fiber and epoxy resin. However, weak interactions between remaining fiber‐matrix occur. Scanning electron microscopy (SEM) analysis was also performed to take some information about strength of interaction between fibers and matrix material. From SEM micrographs, it is concluded that the findings in SEM analysis support to that obtained in FTIR analysis. Another aim of the present work was to investigate the influence of matrix on composite properties. Hence, the strengths of composites having same reinforcement but different matrix systems in axial tension and transverse tension were compared. Short beam shear test has been conducted to characterize the interfacial strength in the composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Mechanical properties of polypropylene composites based on natural fibers subjected to multiple extrusion cycles

The influence of multiple extrusion cycles on the behavior of natural fibers‐reinforced polypropylene was studied. Composites were fabricated with 20 wt % of flax fibers. Final fibers dimensions (length and diameter) were measured by means of optical microscopy. Mechanical properties of matrix and composites were measured after each extrusion cycle. It was observed that the elastic modulus increased by fibers incorporation. The elastic modulus of the matrix was higher after the first process cycle than that of the virgin material, mainly because of chain scission. In the next cycles, the modulus kept constant. On the other hand the elastic modulus of the composite after a single extrusion step was lower than that predicted by the Halpin–Tsai model probably because of a poor mixing and to low adhesion at the fiber–matrix interface. In the following two steps, modulus increased because the better fiber dispersion was observed. For the final two extrusion cycles, the slow decrease in this property was correlated with the darkening and poor organoleptic properties observed as a result of thermal degradation. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 228–237, 2007     

Epoxy hybrid composites cured with octaaminophenyl polyhedral oligomeric silsesquioxane

Polyhedral oligomeric silsesquioxane-containing hybrids of epoxy resins are prepared via the cocuring reaction between octaaminophenyl polyhedral oligomeric silsesquioxane (OAPS) and brominated epoxy resin (EP). The gel time, dispersion, thermal properties, mechanical properties, water absorption, and dielectric properties of the OAPS/EP composites are studied. The gel time of the 1 wt % OAPS composites is significantly higher compared with that of the epoxy resin control. Wide angle X-ray diffraction and scanning electron microscopy show that, at the molecular level, the appropriate amount of POSS cages was dispersed in the epoxy matrix because the POSS monomer participated in the crosslinking reaction. The thermal and mechanical properties of the composites are enhanced as 1 wt % OAPS was added to the epoxy system. The water absorption of the 1 wt % OAPS composite significantly declines. The dielectric constant of the 1 wt % OAPS composite is 0.5 less than that of the epoxy resin control in the range of 100 Hz–40 MHz. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

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     

FRP composites based on different types of glass fibers and matrix resins: A comparative study

Flexural properties, impact energy, heat deflection temperature, and resistance to thermal and hydrothermal degradation of composites based on E-glass and N-glass fibers as the reinforcing agents, and epoxy, unsaturated polyester, phenolic, and epoxy-phenolic resin systems as the matrix materials were studied and compared. As a reinforcing agent E-glass fiber is superior to N-glass fiber, particularly with respect to development of flexural strength and modulus, impact strength, and thermal resistance; N-glass fiber, however, imparts to the composites substantially higher resistance to hydrothermal degradation under boiling conditions in different chemical environments. For use of both E-glass and N-glass fibers as reinforcing agents, the general order of resistance to hydrothermal degradation for the composites based on different matrix resins is epoxy > phenolic > unsaturated polyester resin. Incorporation of a low dose of a rubbery polymer, such as styrene butadiene rubber (0.1–0.2%) and liquid polybutadiene (0.5–0.75%), in unsaturated polyester resin as the matrix resin measurably enhances impact energy of the composite. © 1995 John Wiley & Sons, Inc.     

Morphology and mechanical properties of unidirectional sisal– epoxy composites

Plant fibers are of increasing interest for use in composite materials. They are renewable resources and waste management is easier than with glass fibers. In the present study, longitudinal stiffness and strength as well as morphology of unidirectional sisal–epoxy composites manufactured by resin transfer molding (RTM) were studied. Horseshoe‐shaped sisal fiber bundles (technical fibers) were nonuniformly distributed in the matrix. In contrast to many wood composites, lumen was not filled by polymer matrix. Technical sisal fibers showed higher effective modulus when included in the composite material than in the technical fiber test (40 GPa as compared with 24 GPa). In contrast, the effective technical fiber strength in the composites was estimated to be around 400 MPa in comparison with a measured technical fiber tensile strength of 550 MPa. Reasons for these phenomena are discussed. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 2358–2365, 2002