Dynamic mechanical properties of oil palm microfibril‐reinforced natural rubber composites

The dynamic mechanical properties of macro and microfibers of oil palm‐reinforced natural rubber (NR) composites were investigated as a function of fiber content, temperature, treatment, and frequency. By the incorporation of macrofiber to NR, the storage modulus (E') value increases while the damping factor (tan δ) shifts toward higher temperature region. As the fiber content increases the damping nature of the composite decreases because of the increased stiffness imparted by the natural fibers. By using the steam explosion method, the microfibrils were separated from the oil palm fibers. These fibers were subjected to treatments such as mercerization, benzoylation, and silane treatment. Resorcinol‐hexamethylenetetramine‐hydrated silica was also used as bonding agent to increase the fiber/matrix adhesion. The storage modulus value of untreated and treated microfibril‐reinforced composites was higher than that of macrofiber‐reinforced composites. The T_g value obtained for this microfibril‐reinforced composites were slightly higher than that of macrofiber‐reinforced composites. The activation energy for the relaxation processes in different composites was also calculated. The morphological studies using scanning electron microscopy of tensile fracture surfaces of treated and untreated composites indicated better fiber/matrix adhesion in the case of treated microfibril‐reinforced composites. Finally, attempts were made to correlate the experimental dynamic properties with the theoretical predictions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Dynamical mechanical analysis of sisal/oil palm hybrid fiber‐reinforced natural rubber composites

Natural rubber was reinforced with sisal and oil palm fibers and was subjected to dynamic mechanical analysis to determine the dynamic properties as a function of temperature. The storage modulus E′ was found to increase with weight fraction of fiber. This is due to the increased stiffness imparted by the natural fibers. Loss modulus increased with loading while the damping property was found to decrease. The fibers were subjected to alkali treatment of different concentrations namely 0.5, 1, 2, and 4% and the dynamic properties were studied. In the case of composites containing chemically modified fibers, storage modulus and loss modulus were found to increase. Scanning electron micrographs of tensile fracture surfaces of treated and untreated composites demonstrated better fiber–matrix bonding in the case of the former. POLYM. COMPOS., 27: 671–680, 2006. © 2006 Society of Plastics Engineers     

Study on the effect of woven sisal fiber mat on mechanical and viscoelastic properties of petroleum based epoxy and bioresin modified toughened epoxy network

Sisal fiber reinforced biocomposites are developed using both unmodified petrol based epoxy and bioresin modified epoxy as base matrix. Two bioresins, epoxidized soybean oil and epoxy methyl soyate (EMS) are used to modify the epoxy matrix for effective toughening and subsequently two layers of sisal fiber mat are incorporated to improve the mechanical and thermomechanical properties. Higher strength and modulus of the EMS modified epoxy composites reveals good interfacial bonding of matrix with the fibers. Fracture toughness parameters K_IC and G_IC are determined and found to be enhanced significantly. Notched impact strength is found to be higher for unmodified epoxy composite, whereas elongation at break is found to be much higher for modified epoxy blend. Dynamic mechanical analysis shows an improvement in the storage modulus for bioresin toughened composites on the account stiffness imparted by fibers. Loss modulus is found to be higher for EMS modified epoxy composite because of strong fiber–matrix interfacial bonding. Loss tangent curves show a strong influence of bioresin on damping behavior of epoxy composite. Strong fiber–matrix interface is found in modified epoxy composite by scanning electron microscopic analysis. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42699.     

The effect of fiber concentration on mechanical and thermal properties of fiber‐reinforced polypropylene composites

A novel composite material consisting of polypropylene (PP) fibers in a random poly(propylene‐co‐ethylene) (PPE) matrix was prepared and its properties were evaluated. The thermal and mechanical properties of PP–PPE composites were studied by dynamic mechanical analysis (DMA) and differential scanning calorimetry (DSC) with reference to the fiber concentration. Although, by increasing PP fiber concentration in PPE, no significant difference was found in melting and crystallization temperatures of the PPE, the storage, and the tensile and flexural modulus of the composites increased linearly with fiber concentrations up to 50%, 1.5, 1.0, 1.3 GPa, respectively, which was approximately four times higher than that for the pure PPE. There is a shift in glass transition temperature of the composite with increasing fiber concentration in the composite and the damping peak became flatter, which indicates the effectiveness of fiber–matrix interaction. A higher concentration of long fibers (>50% w/w) resulted in fiber packing problems, difficulty in dispersion, and an increase in void content, which led to a reduction in modulus. Cox–Krenchel and Haplin–Tsai equations were used to predict tensile modulus of random fiber‐reinforced composites. A Cole–Cole analysis was performed to understand the phase behavior of the composites. A master curve was constructed based on time–temperature superposition (TTS) by using data over the temperature range from −50 to 90°C, which allowed for the prediction of very long and short time behavior of the composite. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2260–2272, 2005     

Dynamic mechanical properties of sisal fiber reinforced polyester composites fabricated by resin transfer molding

The dynamic mechanical properties of sisal fiber reinforced polyester composites fabricated by resin transfer molding (RTM) were investigated as a function of fiber content, frequency, and temperature. Investigation proved that at all temperature range the storage modulus (E′) value is maximum for the composites having fiber loading of 40 vol%. The loss modulus (E″) and damping peaks (tan δ) were lowered with increasing fiber content. The height of the damping peaks depends upon the fiber content and the fiber/matrix adhesion. The extent of the reinforcement was estimated from the experimental storage modulus, and it has been found that the effect of reinforcement is maximum at 40 vol% fiber content. As the fiber content increases the T_g from tan δ curve showed a positive shift. The loss modulus, storage modulus, and damping peaks were evaluated as a function of frequency. The activation energy for the glass transition increases upon the fiber content. Cole–Cole analysis was made to understand the phase behavior of the fiber reinforced composites. Finally, attempts were made to correlate the experimental dynamic properties with theoretical predictions. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Wood‐fiber‐reinforced poly(lactic acid) composites: Evaluation of the physicomechanical and morphological properties

This article presents the results of a study of the processing and physicomechanical properties of environmentally friendly wood‐fiber‐reinforced poly(lactic acid) composites that were produced with a microcompounding molding system. Wood‐fiber‐reinforced polypropylene composites were also processed under similar conditions and were compared to wood‐fiber‐reinforced poly(lactic acid) composites. The mechanical, thermomechanical, and morphological properties of these composites were studied. In terms of the mechanical properties, the wood‐fiber‐reinforced poly(lactic acid) composites were comparable to conventional polypropylene‐based thermoplastic composites. The mechanical properties of the wood‐fiber‐reinforced poly(lactic acid) composites were significantly higher than those of the virgin resin. The flexural modulus (8.9 GPa) of the wood‐fiber‐reinforced poly(lactic acid) composite (30 wt % fiber) was comparable to that of traditional (i.e., wood‐fiber‐reinforced polypropylene) composites (3.4 GPa). The incorporation of the wood fibers into poly(lactic acid) resulted in a considerable increase in the storage modulus (stiffness) of the resin. The addition of the maleated polypropylene coupling agent improved the mechanical properties of the composites. Microstructure studies using scanning electron microscopy indicated significant interfacial bonding between the matrix and the wood fibers. The specific performance evidenced by the wood‐fiber‐reinforced poly(lactic acid) composites may hint at potential applications in, for example, the automotive and packaging industries. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4856–4869, 2006     

Dynamic mechanical analysis and morphological studies of fly ash/mica reinforced poly(ether‐ether‐ketone)‐based hybrid composites

Hybrid composites based on poly(ether‐ether‐ketone) (PEEK) were fabricated with fly ash and mica. Nearly 5, 10, and 15 wt% of fly ash were replaced by mica of the optimized fly ash reinforced composites and were subjected to dynamical mechanical analysis to determine the dynamic properties as a function of temperature. The storage modulus E′ was found to decrease with the increase of weight fraction of mica. Loss modulus was also found to decrease with loading while the damping property was found to increase marginally. Peak height of tan δ for hybrid composites were decreased by varying combinations of fly ash with mica. It is probably due to improved crystallinity of PEEK and strong interaction between the fillers and PEEK matrix. Cole–Cole analysis was made to understand the phase behavior of the composite samples. Kubat parameter was calculated to study the adhesion between matrix and filler of the fabricated composites. Without surface modification for inorganic fillers, the distribution of two different shape filler particles appears to be reasonably uniform. The use and limitation of various theoretical equations to predict the tan δ and storage modulus of filler reinforced composites have been discussed. Addition of both fillers opens up new opportunities for development of high‐performance multifunctional materials suitable for industrial applications. Scanning electron micrographs of tensile fracture surfaces of composites demonstrated filler–matrix bonding. POLYM. COMPOS., 35:68–78, 2014. © 2013 Society of Plastics Engineers     

Influence of fiber treatment on the performance of sisal–polypropylene composites

This article concerns the effectiveness of MAPP as a coupling agent in sisal–polypropylene composites. The fiber loading, MAPP concentration, and fiber treatment time influenced the mechanical properties of the composites. It was observed that the composites prepared at 21 volume percent of fibers with 1% MAPP concentration exhibits optimum mechanical strength. SEM investigations confirmed that the increase in properties is caused by improved fiber‐matrix adhesion. The viscoelastic properties of the treated and untreated composites were also studied. From the storage modulus versus temperature plots, an increase in the magnitude of the peaks was observed with the addition of MAPP and fiber reinforcement, thus showing an improvement in stiffness of the treated composites. The damping properties of the composites, however, decreased with the addition of the fibers and MAPP. The thermal properties of the composites were analyzed through DSC and TGA measurements. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1336–1345, 2004     

Dynamic mechanical properties of oil palm fiber/phenol formaldehyde and oil palm fiber/glass hybrid phenol formaldehyde composites

The dynamic mechanical properties of oil palm fiber reinforced phenol formaldehyde (PF) composites and oil palm/glass hybrid fiber reinforced PF composites were investigated as a function of fiber content and hybrid fiber ratio. The dynamic modulus of the neat PF sample decreases with decrease in frequency. Glass transition attributed with the α relaxation of the neat PF sample was observed around 140°C. Tanδ values and storage modulus show great enhancement upon fiber addition. The value increases with increase in fiber content. The loss modulus shows a reverse trend with increase in fiber loading. Incorporation of oil palm fiber shifts the glass transition towards lower temperature value. The glass transition temperature of the hybrid composites is lower than that of the unhybridized composites. The highest value of mechanical damping is observed in hybrid composites. Storage modulus of the hybrid composites is lower than unhybridized oil palm fiber/PF composite. A similar trend is observed for loss modulus. Activation energies for the relaxation processes in different composites were calculated. Activation energy is increased upon fibrous reinforcement. Complex modulus variations and phase behavior of the composites were studied from Cole‐Cole plots. Finally, master curves for the viscoelastic properties of the composites were constructed on the basis of time‐temperature superposition principle. POLYM. COMPOS., 26:388–400, 2005. © 2005 Society of Plastics Engineers     

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     

Analysis of the tensile modulus of poly(p‐hydroxybenzoate)/poly(ethylene terephthalate)/poly(ethylene 2,6‐naphthalate) ternary polyester composite fibers

Liquid crystalline polymer reinforced plastics were prepared by compounding (PHB/PEN/PET) blends. A fibrillar PHB structure was formed in situ in the PEN/PET matrix under a high elongational flow field during melt‐spinning of the composite fibers. The formation of PHB microfibrils in the composite fiber with different PHB contents and winding speeds was observed. The PHB microfibril reinforced PEN/PET composite fibers exhibited an unexpectedly low tensile modulus. We have evaluated the tensile modulus of the fibers using the non‐modified 22 and a modified 23 Halpin–Tsai model. From the analysis of both models, large differences were found between the theoretical and experimental values of the tensile modulus, and the low value of the tensile modulus of the composite fiber could not adequately be explained by either model. Thus, we analyzed the observed modulus values using the Takayanagi model, 24 which describes the concept of mechanical discontinuities in semi‐crystalline polymers. Using the Takayanagi model, the effective fraction of continuous or discontinuous microfibrils was evaluated. Consequently, we could successfully explain the very low modulus of the PHB/PEN/PET composite fiber, having a large number of PHB microfibrils, using the Takayanagi model. Copyright © 2003 Society of Chemical Industry     

A dynamic mechanical study on unidirectional carbon fiber-reinforced polypropylene composites

Fiber-reinforced polymer composites show high specific strength and stiffness. The alignment of reinforcing fibers results in anisotropy of the material. This anisotropic behavior has been studied through dynamic mechanical analysis of unidirectional carbon fiber-reinforced polypropylene (CFRPP) composites measured in both parallel and transverse directions to fiber arrangement. Several parameters such as storage modulus (E′), loss modulus (E″), loss factor or damping factor (tan δ), and complex viscosity (MU^*) have been determined over a wide range of frequencies and at a fixed temperature. Relaxation and retardation spectra have been constructed for these composites. Modulus enhancement occurs due to stiffness imparted by the fiber and efficient stress transfer at the interface. Relaxation of the polymer matrix ceases with increase in the volume fraction of the fibers. α′-relaxation is observed for the composite having a 13% volume fraction of fibers and is ascribed to relaxation in the crystalline phase where the additional crystallinity arises out of the transcrystalline growth at the fiber–matrix interface. There exists a good correlation between theroretical curves with the experimental ones. Relaxation and retardation spectra and the dynamic parameters determined for these composites show a good correlation with the volume fraction of fibers as well as the direction of the applied load. © 1994 John Wiley & Sons, Inc.     

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     

Rheological characterization of PP/jute composite melts

The present article summarizes an experimental study on the molten viscoelastic behavior of PP/jute composites under steady and dynamic mode. Variations in melt viscosity and die swell of the composites with an increase in shear rate, fiber loading, and coupling agent concentration have been investigated using capillary rheometer. It was observed that with the addition of fibers and MAPP, the melt viscosity of the composites increased due to improved fiber‐matrix interfacial adhesion. Further, the dynamic viscoelastic behavior, measured using parallel plate rheometer, revealed an increase in the storage modulus (G′), indicating higher stiffness in case of fiber‐filled composites as compared with the virgin matrix. Time–temperature superposition was applied to generate various viscoelastic master curves. The fiber‐matrix morphology of the extrudates was also examined using scanning electron microscopy, which corroborated the findings of rheological properties. The treated composites displayed uniform distribution of fibers within the PP matrix with lesser surface irregularities. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1476–1484, 2006     

Investigation of the dynamic mechanical behavior of polypropylene/(wood flour)/(kenaf fiber) hybrid composites

Polypropylene/(wood flour)/(kenaf fiber) hybrid composites were prepared in an internal mixer. Kenaf was considered as a fibrous filler and wood flour as a particulate filler. The lignocellulosic loading used was 50%. Dynamic mechanical thermal analysis properties such as storage modulus (E′), loss modulus (E″), damping factor (tan δ), and adhesion factor were evaluated. It was found that the adhesion factor could interpret the interfacial adhesion between lignocellulosic fillers and the plastic matrix macroscopically. This factor was affected by the type of filler used and the coupling agent concentration. The variation of storage modulus was affected more by the shape of the filler and the coupling agent concentration at higher temperatures than at temperatures below the glass transition. Owing to a higher probability of agglomeration in a sample containing 50 wt% of wood flour, the storage modulus and complex viscosity of this sample were higher than those of other samples. Cole‐Cole diagrams showed that the homogeneity of samples containing a higher amount of coupling agent was higher than that of samples with a lower concentration. J. VINYL ADDIT. TECHNOL., 2009. © 2009 Society of Plastics Engineers     

Banana/Glass Fiber-Reinforced Polypropylene Hybrid Composites: Fabrication and Performance Evaluation

Hybrid composites of Polypropylene (PP) reinforced with intimately mixed short banana and glass fibers were fabricated using Haake twin screw extruder followed by compression molding with and without the presence maleic anhydride grafted polypropylene (MAPP) as a coupling agent. Incorporation of both the fibers into PP matrix resulted in an increase in tensile, flexural and impact strength with an increasing level of fiber content upto 30 wt% at banana: glass fiber ratio of 15:15 wt% and 2 wt% of MAPP. The rate of water absorption for the hybrid composites decreased due to the presence of glass fiber and coupling agent. The effect of fiber loading in presence of coupling agent on the dynamic mechanical properties has also been analyzed to investigate the interfacial properties. An increase in the storage modulus (E′) of the treated composite indicates higher stiffness. The tan δ spectra confirms a strong influence of fiber contents and coupling agent on the α and β relaxation processes of PP. The nature of fiber matrix adhesion was examined through scanning electron microscopy (SEM) of the tensile fractured specimen. Thermal measurements were carried out employing differential scanning calorimetry (DSC) and the thermogravimetric analysis (TGA) which indicated a decrease in the crystallization temperature and thermal stability of PP with the incorporation of MAPP treated banana and Glass fiber.     

Influence of interfacial adhesion on the structural and mechanical behavior of PP‐banana/glass hybrid composites

Hybrid composites of polypropylene (PP), reinforced with short banana and glass fibers were fabricated using Haake torque rheocord followed by compression molding with and without the presence maleic anhydride grafted polypropylene (MAPP) as a coupling agent. Incorporation of both fibers into PP matrix resulted in increase of tensile strength, flexural strength, and impact strength upto 30 wt% with an optimum strength observed at 2 wt% MAPP treated 15 wt% banana and 15 wt% glass fiber. The rate of water absorption for the hybrid composites was decreased due to the presence of glass fiber and coupling agent. The effect of fiber loading in presence of coupling agent on the dynamic mechanical properties has been analyzed to investigate the interfacial properties. An increase in storage modulus (E′) of the treated‐composite indicates higher stiffness. The loss tangent (tan δ) spectra confirms a strong influence of fiber loading and coupling agent concentration on the α and β relaxation process of PP. The nature of fiber matrix adhesion was examined through scanning electron microscopy (SEM) of the tensile fractured specimen. Thermal measurements were carried out through differential scanning calorimetry (DSC) and the thermogravimetric analysis (TGA), indicated an increase in the crystallization temperature and thermal stability of PP with the incorporation of MAPP‐treated banana and glass fiber. POLYM. COMPOS., 31:1247–1257, 2010. © 2009 Society of Plastics Engineers     

Oil palm microcomposites: Processing and mechanical behavior

The present work focuses on the effect of concentration and modifications of oil palm microfibrils in natural rubber. Increase in the concentration of microfibrils resulted in the reduction of tensile and tear strengths while an increase in modulus, hardness, and abrasion resistance of composites. The extent of microfibril orientation in the composite was determined from green strength measurements. Microcomposites were also prepared by using fibrils treated with benzoyl chloride, silane coupling agent, and hydrated silica‐resorcinol‐hexamethylenetetramine bonding agent. The treated and untreated microfibrils were characterized by FTIR. Scanning electron micrograph studies were carried out to analyze the microfibril pull out and fiber/matrix adhesion of composites. The extent of fiber alignment and interfacial adhesion were analyzed from swelling measurements. Finally, experimental results of mechanical properties were compared with the theoretical predictions. POLYM. ENG. SCI., 50:1853–1863, 2010. © 2010 Society of Plastics Engineers     

Polyphenylene sulphide/carbon fiber composites: study on their thermal,mechanical and microscopic properties

The present study investigates the thermal, mechanical and microscopic properties of polyphenylene sulphide/carbon fiber (PPS/CF) composites by incremental number of fiber layers. The composites were prepared by hand lay-up technique followed by compression molding. A superior matrix-reinforcement adhesion was attained without the use of coupling agent and mechanical stability of the composites improved with increasing fiber layers. Transverse rupture strength and bending modulus were improved by 59.84 and 125.21 %, respectively, without loss in toughness. Impact strength and hardness values were enhanced while storage modulus, loss modulus and damping factor were dropped by increases in fiber layers. Thermogravimetric analysis (TGA) indicated a gradual rise in thermal stability (16.84 %) of the composite as compared to pure matrix. Surface morphology and crack propagation were studied by optical microscopy. It was found that crack was propagated in a linear plane by applying load. In addition, scanning electron microscopy (SEM) illustrated steady alignment of fibers and uniform distribution of the matrix around reinforcement. Based on the obtained results, fiber layers showed great potential for enhancement of thermal and mechanical properties of the composites.     

Mechanical properties and morphology of flax fiber reinforced melamine‐formaldehyde composites

The mechanical performance of natural fiber reinforced polymers is often limited owing to a weak fiber‐matrix interface. In contrast, melamine‐formaldehyde (MF) resins are well known to have a strong adhesion to most cellulose containing materials. In this Paper, nonwoven flax fiber mat reinforced and particulate filled MF composites processed by compression molding are studied and compared to a similar MF composite reinforced with glass fibers. Using flax instead of glass fibers has a somewhat negative effect on tensile performance. However, the difference is relatively small, and if density and material cost are taken into account, flax fibers become competitive. Tensile damage is quantified from the stiffness reduction during cyclic straining. Compared to glass fibers, flax fibers generate a material with a considerably lower damage rate. From scanning electron microscopy (SEM), it is found that microcracking takes place mainly in the fiber cell walls and not at the fiber‐matrix interface. This suggests that the fiber‐matrix adhesion is high. The materials are also compared using dynamic mechanical thermal analysis (DMTA) and water absorption measurements.