An investigation of sound absorption coefficient on sisal fiber poly lactic acid bio‐composites

In this research, the mechanical, acoustical, thermal, morphological, and infrared spectral properties of untreated, heat and alkaline‐treated sisal fiber‐reinforced poly‐lactic‐acid bio‐composites were analyzed. The bio‐composite samples were fabricated using a hot press molding machine. The properties mentioned above were evaluated and compared with heat‐treated and alkaline‐treated sisal fibers. Composites with heat‐treated sisal fibers were found to exhibit the best mechanical properties. Thermo‐gravimetric analysis (TGA) was conducted to study the thermal degradation of the bio‐composite samples. It was discovered that the PLA‐sisal composites with optimal heat‐treated at 160°C and alkaline‐treated fibers possess good thermal stability as compared with untreated fiber. The results indicated that the composites prepared with 30wt % of sisal had the highest sound absorption as compared with other composites. Evidence of the successful reaction of sodium hydroxide and heat treatment of the sisal fibers was provided by the infrared spectrum and implied by decreased bands at certain wavenumbers. Observations based on scanning electron microscopy of the fracture surface of the composites showed the effect of alkaline and heat treatment on the fiber surface and improved fiber‐matrix adhesion. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42470.     

A comparative study on the mechanical and degradation properties of plant fibers reinforced polyethylene composites

Coir and abaca fiber‐reinforced linear low density polyethylene (LLDPE) composites (30 wt% fiber) were prepared by compression molding. Coir and abaca fibers were treated with methyl methacrylate (MMA) using ultraviolet radiation to improve the mechanical properties of the composites. Concentration of MMA and radiation dose was optimized. It was found that 30% MMA in methanol along with photoinitiator Darocur‐1173 (2%) and 15th pass of radiation rendered better performance. Chemically treated fiber‐reinforced specimens yielded better mechanical properties compared to the untreated composites, whereas coir fiber composites had better mechanical properties than abaca fiber reinforced ones. For the improvement of the properties, optimized coir (coir fiber treated with 30% MMA) and abaca (abaca fiber treated with 40% MMA) fibers were again treated with aqueous starch solution (2%–8%, w/w) for 2–7 min. Composites made of 3%‐starch‐treated coir fiber (5 min soaking time) showed the best mechanical properties than that of abaca‐fiber‐based composites. Water uptake and soil degradation tests of the composites were also performed. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Recycled milk pouch and virgin low‐density polyethylene/linear low‐density polyethylene based coir fiber composites

The viability of the thermomechanical recycling of postconsumer milk pouches [a 50 : 50 low‐density polyethylene/linear low‐density polyethylene (LDPE–LLDPE) blend] and their use as polymeric matrices for coir‐fiber‐reinforced composites were investigated. The mechanical, thermal, morphological, and water absorption properties of recycled milk pouch polymer/coir fiber composites with different treated and untreated fiber contents were evaluated and compared with those of virgin LDPE–LLDPE/coir fiber composites. The water absorption of the composites measured at three different temperatures (25, 45, and 75°C) was found to follow Fickian diffusion. The mechanical properties of the composites significantly deteriorated after water absorption. The recycled polymer/coir fiber composites showed inferior mechanical performances and thermooxidative stability (oxidation induction time and oxidation temperature) in comparison with those observed for virgin polymer/fiber composites. However, a small quantity of a coupling agent (2 wt %) significantly improved all the mechanical, thermal, and moisture‐resistance properties of both types of composites. The overall mechanical performances of the composites containing recycled and virgin polymer matrices were correlated by the phase morphology, as observed with scanning electron microscopy. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Polypropylene composites reinforced with untreated and chemically treated coir: Effect of the presence of compatibilizer

The effect of coir surface modification on the compatibility of polypropylene (PP)/coir fiber (CF) composites, in the presence and absence of compatibilizer (maleic anhydride grafted polypropylene, PP‐g‐MA) was assessed. Chemical pulping of the fibers was performed with 2, 4, 8, and 12% NaOH solutions for a period of 2 h at (100 ± 4)°C. Pressed composite samples were subjected to tensile testing, scanning electron (SEM) and atomic force microscopy (AFM). Lignin and holocellulose concentrations of untreated and treated coir were determined. Pulping resulted in increased tensile strength of the composites containing coir treated with up to 2% NaOH, due to increased fiber roughness as evidenced by AFM. This property decreased when higher NaOH concentrations were used, likely due to increased deterioration of coir. The presence of compatibilizer in the PP composites containing treated coir altered adhesion due to chemical changes of the fiber surface. At high NaOH concentrations increased delignification and therefore increased exposure of hydroxyls favors reaction between the fiber hydroxyls and the carboxyl acids of the hydrolyzed maleic anhydride, present in the composites. POLYM. ENG. SCI., 55:2050–2057, 2015. © 2014 Society of Plastics Engineers     

Effects of fiber‐surface treatment on the properties of hybrid composites prepared from oil palm empty fruit bunch fibers,glass fibers,and recycled polypropylene

In this article, we report the effects of hybridization and fiber‐surface modification on the properties of hybrid composites prepared from recycled polypropylene (RPP), coupling agents, oil palm empty fruit bunch (EFB), and glass fibers through a twin‐screw extruder and an injection‐molding machine. The surface of the EFB fibers was modified with different concentrations (10–15 wt %) and temperatures (60–90°C) of alkali solutions. The structure and morphology of the fibers were observed with the help of Fourier transform infrared spectroscopy and scanning electron microscopy. Different types of composites were fabricated with untreated, alkali‐treated, and heat‐alkali‐treated fibers. Comparative analysis of the mechanical, structural, morphological, and thermal properties of the composites was carried out to reveal the effects of treatment and hybridization. The analysis results reveal that composites prepared from the alkali‐treated (in the presence of heat) fibers show improved mechanical, thermal, and morphological properties with a remarkably reduced water absorption. Additionally, the crystallinity of RPP also increased with the development of biaxial crystals. The improvement of various properties in relation to the structures and morphologies of the composites is discussed. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43049.     

Scanning electron microscopy study of chemically modified coir fibers

Chemical‐surface modification of coir fibers was done by dewaxing, using an alkali treatment (5% and 10% NaOH), vinyl grafting with methyl methacrylate (MMA) and cyanoethylation. The chemically modified fibers were characterized by Fourier transform infrared (FTIR) spectroscopy. In addition, the surface features of untreated, dewaxed, alkali‐treated, grafted, and cyanoethylated coir fibers were studied using scanning electron microscopy (SEM). Progressive changes in surface morphology were observed. SEM observations showed the removal of tyloses from the surface of coir as a result of alkali treatment (5%), resulting in a rough fiber surface with regularly spaced pits. At a lower percentage of grafting (PMMA), the surfaces became more or less uniform, while the surfaces of the coir fibers with a higher percentage of grafting were increasingly covered with grafted materials, resulting in canal‐like cavities between the overgrowths of the grafted materials on the unit cells. Cyanoethylated coir‐fiber surfaces showed an insufficient deposit of cyanoethyl groups. SEM analysis of the samples was corroborated by measurements of a mechanical property (maximum stress at break). © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1169–1177, 2001     

High‐performance copoly(benzimidazole‐benzoxazole‐imide) fibers: Fabrication,structure, and properties

Novel high‐performance copolyimide (co‐PI) fibers containing benzimidazole and benzoxazole ring in the main chain were prepared by a two‐step spinning via the poly(amic acid)s. Effects of the incorporated benzimidazole and benzoxazole units on the micro‐structure and properties of co‐PI fibers were investigated. Fourier transform infrared (FTIR) results indicated that hydrogen bonding is formed in the co‐PI fibers. The co‐PI fibers exhibited discernible crystallization peaks at 14°～15° and 23°～26° (2θ), showing crystalline‐like structure. Moreover, the packing type of benzimidazole‐imide units determined the macromolecules packing of co‐PIs. It was amazedly found that the co‐PI fibers exhibited higher tensile strength and initial modulus than those of corresponding homo‐PI fibers, reaching tensile strength of 2.2–2.6 GPa, initial modulus of 99.1–113.2 GPa. The results of dynamic mechanical analysis (DMA) indicated co‐PI2 fiber had a positive T_g deviation due to the presence of strong intermolecular hydrogen bonding between benzimidazole‐imide and benzoxazole‐imide units, which maybe lead to the effective stress transfer between benzimidazole‐imide units and benzoxazole‐imide units. In addition, the obtained PI fibers exhibited excellent thermal properties with the 10% weight loss temperatures under N₂ in the range of 574–585°C. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42001.     

Cellulosic nanocomposites. II. Studies by atomic force microscopy

Dissolving‐grade wood pulp fibers were partially esterified by mixed p‐toluene sulfonic/hexanoic acid anhydride in a nonswelling suspending agent. A biphasic morphology was revealed by atomic force microscopy (AFM) for the compression‐molded, partially modified pulp fibers. The AFM phase images indicated distinct periodicity on the scale of several 10's of nanometers. Surface etching with cellulolytic enzymes of the modified pulp fibers produced height images that had virtually the same periodicity. These results indicate that the modified pulp fibers are nanocomposites comprising unmodified cellulose and cellulose hexanoate. Regenerated lyocell fibers (from N,MMNO solvent) subjected to the same esterification system as applied to pulp fibers, by contrast, exhibited AFM phase images that indicated a high level of surface (skin) versus core reactivity. Modified lyocell fibers with an average diameter of about 12 μm and having an overall DS of 0.6 had surface layers that were approximately 1 μm thick. The latter represented a transitional phase in which the chemical composition and the physical properties were intermediate between a highly substituted surface (skin) and an unsubstituted core. When a compression‐molded sheet of the modified lyocell fibers was analyzed by microthermal analysis, the thermoplastic matrix on the lyocell fiber surface was revealed to have an apparent T_g of 75°C corresponding to cellulose hexanoate, whereas no significant thermal transition was determined for the (unmodified) fiber core. These results suggest that both partially modified lyocell fibers and partially modified pulp fibers are capable of producing composites with morphologies that have grossly different scales. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 2254–2261, 2000     

Effect of thermal annealing on the mechanical and thermal properties of polylactic acid–cellulosic fiber biocomposites

Polylactic acid (PLA) biocomposites were produced by a combination of extrusion and injection molding with three cellulosic reinforcements (agave, coir, and pine) and contents (10, 20, and 30%). In particular, some samples were subjected to thermal annealing (105 °C for 1 h) to modify the crystallinity of the materials. In all cases, morphological (scanning electron microscopy) and thermal (differential scanning calorimetry, dynamical mechanical thermal analysis) characterizations were related to the mechanical properties (Charpy impact, tensile and flexural tests). The results showed that annealing increased the crystallinity for all the materials produced, but different mechanical behaviors were observed depending on fiber type and content. For example, annealing increased the impact strength and flexural modulus of PLA and PLA biocomposites (agave, coir, and pine), while decreasing their flexural strength. But the main conclusion is that fiber addition combined with thermal annealing can substantially increase the thermal stability of the studied materials. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43750.     

Biodegradable composites: Morphological,chemical, thermal,and mechanical properties of composites of poly(hydroxybutyrate‐co‐hydroxyvalerate) with curaua fibers after exposure to simulated soil

Composites produced from biodegradable polymeric matrixes reinforced with vegetable fibers have attractive mechanical properties and are environmentally friendly. This work is directed to the biodegradation of a composite made of a poly(hydroxybutyrate‐co‐hydroxyvalerate) matrix reinforced with curaua fibers (with and without alkaline treatment) in simulated soil. The composites were developed by extrusion and injection and were later buried in simulated soil according to the ASTM G160‐03 method. Scanning electron microscopy showed evidence of microbial attack on the samples surfaces. Infrared spectra showed that the composites biodegradation was mainly caused by erosion of the surface layer resulting from microorganisms activity. Thermogravimetric analysis pointed out reduced thermal stability of the samples, and results of differential scanning calorimetry showed that the degree of crystallinity increases and then decreases progressively throughout the degradation period, indicating that enzymatic degradation primarily occurs in the amorphous phase material and thereafter in the crystalline phase. For curaua composite fibers, reductions in tensile strength and elastic modulus are more significant, indicating that the presence of fibers promotes biodegradation of the curaua fiber. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40712.     

Investigation on the use of coir fiber as alternative reinforcement in polypropylene

Polypropylene/coir fiber composites were prepared according to an experimental statistical design, in which the independent variables, coir fiber, and compatibilizer content, were varied. The compatibilizer used was maleic anhydride grafted polypropylene (PP‐g‐MA). Compatibilizer free composites were also prepared. Composites were processed in a corotating twin‐screw extruder and submitted to mechanical and morphological analyses. The effects of the independent variables on the mechanical properties were assessed through tensile strength, elongation at break, flexural modulus, and impact strength. The morphological properties were assessed by scanning electron microscopy (SEM). The results indicated the need for using compatibilizers in the composites due to the incompatibility of PP and coir fiber. The variable with the strongest effect on the properties was coir content, whose increase caused increase in tensile strength, impact strength and elastic modulus, and decrease in elongation at break. The presence of PP‐g‐MA was fundamental to achieving the aforementioned results. The effect of increasing compatibilizer content was only observed for the elastic modulus. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Influence of iodine treatment on the carbonization behavior of Antheraea pernyi silk fibroin fiber

The effect of iodine treatment on the carbonization behavior of tussah silk fibroin (SF) fiber from a wild cocoon, Antheraea pernyi (A. pernyi), was investigated, and the carbon yield, fiber morphology, structural characteristics, and mechanical properties were evaluated. The SF fiber was treated with iodine vapor at 100°C for 12 h and was heated to 800°C under a multistep heating program as carbonization process, which corresponds to the constant thermal degradation rate of SF determined by dynamic thermogravimetric analysis (TGA). The carbon yield was ca. 39 wt %, which is much higher than those for untreated A. pernyi. Scanning electron microscopic (SEM) observation showed that obtained carbon fibers from iodinated SF were structurally intact, and the strength was higher than that from untreated SF. Fourier transform infrared spectroscopy (FTIR), X‐ray diffraction, and Raman spectroscopy revealed that the structures of the carbon fibers obtained from both untreated and iodinated SF were almost the same and amorphous. At the early stage of carbonization of SF, amide bonding of SF molecules was begin to collapse at temperatures higher than 350°C and was completely dissociated by carbonization at 800°C. Dynamic viscoelastic measurements showed that with heating above 270°C the iodine component introduced intermolecular crosslinking of SF and the melt flow of the SF was inhibited, which enhances higher carbon yield and better performance of silk based carbon fiber. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Mechanical,morphological, and thermal properties of chemically treated pine needles reinforced thermosetting composites

Natural fibers are widely used as reinforcement in composites. Pine needles are one of the major biowaste generated by Pinus roxburgii plant. This species is found abundantly in the forests of Himachal Pradesh. In this work, composites of urea–resorcinol–formaldehyde resin‐reinforced with Pine needles fibers were prepared. Fibers were chemically modified to improve their compatibility with matrix. These fibers were mercerized with NaOH solution and acetylated to increase their hydrophobic character. The chemically modified fibers were characterized with Fourier transform infrared spectra, ¹³C‐nuclear magnetic resonance (NMR) spectroscopy, and scanning electron microscopy. The composites were prepared with treated and untreated fibers containing 30% fibers by weight using compression molding technique. The morphology of the materials thus obtained was evaluated by scanning electron microscopy. The chemical modifications of fibers improve fiber–matrix adhesion and also have markedly effect on mechanical properties of composites. Moreover, the thermal resistance of these composites was improved on chemical modification. These results indicate that chemically modified fibers exhibit better compatibility with the polymer matrix than that of untreated fiber. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci, 2013     

Effect of nonionizing radiation on the physicomechanical properties of banana fiber/pp composites with HEMA

Banana fiber‐reinforced polypropylene (PP)‐based unidirectional composites (40% fiber by weight) was manufactured by compression molding. Banana fibers and PP sheets were treated with UV radiation at different intensities and then composites were fabricated. It was found that mechanical properties of irradiated banana fiber and irradiated PP‐based composites were found to increase significantly compared to that of untreated counterparts. Irradiated banana fibers were also treated with 2‐hydroxyethyl methacrylate (HEMA) mixed with methanol (MeOH) under thermal curing method at different temperatures (30–70°C) for different curing times (20–60 min). A series of solutions of different concentrations of HEMA in methanol along with 2% benzyl peroxide were prepared. Monomer concentration, curing temperature and curing time were optimized in terms of polymer loading and mechanical properties. Composites made of 15% HEMA, 50°C and 40 min curing time showed the best mechanical properties than those of untreated composite. Scanning electron microscopy (SEM), water uptake, and simulating weathering test of the composites were also investigated. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Structure–property relationship of polyimide fibers containing ether groups

The copolyimide (co‐PI) fibers with outstanding mechanical properties were prepared by a two‐step wet‐spinning method, derived from the design of combining 4,4′‐oxydianiline (ODA) with the rigid 3,3′,4,4′‐biphenyltetracarboxylic dianhydride (BPDA)/p‐phenylenediamine (p‐PDA) backbone. The mechanical properties of PI fibers were drastically improved with the optimum tensile strength of 2.53 GPa at a p‐PDA/ODA molar ratio of 5/5, which was approximately 3.7 times the tensile strength of BPDA/p‐PDA PI fibers. Two‐dimensional wide‐angle X‐ray diffraction indicated that the highly oriented structures were formed in the fibers. Two‐dimensional small‐angle X‐ray scattering revealed the existence of the needle‐shaped microvoids aligned parallel to the fiber axis, and the introduction of ODA led to the reduction in the size of the microvoids. As a result, the significantly improved mechanical properties of PI fibers were mainly attributed to the gradually formed homogeneous structures. The co‐PI fibers also exhibited excellent thermal stabilities of up to 563°C in nitrogen and 536°C in air for a 5% weight loss and glass transition temperatures above 279°C. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42474.     

Effect of treatment pressure on structures and properties of PMIA fiber in supercritical carbon dioxide fluid

The effects of treatment pressure on the structures and properties of PMIA fiber were investigated by Scanning electron microscopy, Dynamic wetting measurements, Fourier transform infrared spectrometry, X‐ray diffraction, thermogravimetric analysis, and mechanical properties test technology in supercritical carbon dioxide. The results indicated that the surface morphology, the water contact angle, the interaction of macromolecules, the crystal structure, the thermal property, and tensile strength of PMIA fibers were changed during supercritical carbon dioxide treatment, particularly the surface morphology and the wettability of fiber changed the most obviously with the increase of treatment pressure. Furthermore, the thermal property and tensile strength of treated PMIA fiber sample were improved in comparison with those of untreated sample. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41756.     

Influence of alkali fiber treatment and fiber processing on the mechanical properties of hemp/epoxy composites

Industrial hemp fibers were treated with a 5 wt % NaOH, 2 wt % Na₂SO₃ solution at 120°C for 60 min to remove noncellulosic fiber components. Analysis of fibers by lignin analysis, scanning electron microscopy (SEM), zeta potential, Fourier transform infrared (FTIR) spectroscopy, wide angle X‐ray diffraction (WAXRD) and differential thermal/thermogravimetric analysis (DTA/TGA), supported that alkali treatment had (i) removed lignin, (ii) separated fibers from their fiber bundles, (iii) exposed cellulose hydroxyl groups, (iv) made the fiber surface cleaner, and (v) enhanced thermal stability of the fibers by increasing cellulose crystallinity through better packing of cellulose chains. Untreated and alkali treated short (random and aligned) and long (aligned) hemp fiber/epoxy composites were produced with fiber contents between 40 and 65 wt %. Although alkali treatment generally improved composite strength, better strength at high fiber contents for long fiber composites was achieved with untreated fiber, which appeared to be due to less fiber/fiber contact between alkali treated fibers. Composites with 65 wt % untreated, long aligned fiber were the strongest with a tensile strength (TS) of 165 MPa, Young's modulus (YM) of 17 GPa, flexural strength of 180 MPa, flexural modulus of 9 GPa, impact energy (IE) of 14.5 kJ/m², and fracture toughness (K_Ic) of 5 MPa m^1/2. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Surface modification of coir fibers. II. Cu(II)‐ IO initiated graft copolymerization of acrylonitrile onto chemically modified coir fibers

A study of the graft copolymerization of acrylonitrile (AN) onto chemically modified coir fibers was carried out using a CuSO₄ and NaIO₄ combination as the initiator in an aqueous medium in a temperature range of 50–70°C. The graft yield was influenced by the reaction time, temperature, concentration of CuSO₄, concentration of NaIO₄, and monomer concentration. Grafting was also carried out in the presence of inorganic salts and organic solvents. A combination of copper(II) and sodium periodate (Cu²⁺‐IO) in an aqueous medium with an IO concentration of 0.005 mol L^?1 and a Cu²⁺ concentration of 0.004 mol L^?1 produced optimum grafting. The chemically modified and AN grafted fibers were characterized by FTIR and scanning electron microscopy (SEM). The SEM studies revealed that grafting not only takes place on the surface of the fibers but also penetrates the fiber matrix. The tensile properties like the maximum stress at break and extension at break of untreated, chemically modified, and AN grafted coir fibers were evaluated and compared. The extent of absorption of water of untreated, chemically modified, and grafted coir fibers was determined. It was found that grafting of AN imparts hydrophobicity onto coir fibers. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 84: 75–82, 2002; DOI 10.1002/app.10221     

Fundamental influences on quasistatic and cyclic material behavior of short glass fiber reinforced polyamide illustrated on microscopic scale

In this work, the influences of fiber orientation and weld lines on the morphological structures and the mechanical behavior of polyamide 6.6 (PA6.6‐GF35) are investigated. In quasistatic and fatigue tests tensile and 3‐point‐bending loads are applied. Test temperatures vary between RT and 150°C. Two different specimen types are produced by using injection moulding process to create different fiber orientations as well as weld lines. Fiber orientations are determined using computer tomography. Scanning electron microscopy is used to investigate fracture surfaces of tested specimens. Results show that mechanical properties and morphological structures depend highly on fiber orientation and temperature. Transversely oriented fibers in weld lines result in brittle failure mechanisms and decreased mechanical properties. Different stress distributions in the specimens under tensile and flexural loads have influence on the material behavior as well. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40842.     

Effects of poly(dimethyl siloxane) on the water absorption and natural degradation of poly(lactic acid)/oil‐palm empty‐fruit‐bunch fiber biocomposites

Composites were fabricated with poly(lactic acid) and oil‐palm empty‐fruit‐bunch (EFB) fibers with extrusion; this was followed by an injection‐molding technique. Before compounding, the surface of the fiber was modified through ultrasound and poly(dimethyl siloxane) (PDMS). The influences of the ultrasound and PDMS on the water absorption and biodegradability of the composites were investigated. Additionally, the composites were buried under soil for 6 months, and their biodegradability was assessed through different characterization techniques, such as tensile testing and weight loss and diffussability measurement. The changes on the surface of the fibers due to treatment were examined by scanning electron microscopy analysis, and the influences on the biodegradability of the composites were observed. Functional group analysis and possible changes before and after degradation were also examined by a Fourier transform infrared spectrophotometric technique. The results analyses revealed that the treatment of fibers improved the density of the fibers and reduced the water uptake of the composites. The overall weight loss due to soil burial testing was found to be maximum for the untreated‐fiber‐based composites (6.8%), whereas the ultrasound‐ and silane‐treated composites showed the minimum value of weight loss (3.7%). The deterioration of the tensile strength due to degradation was found to be at a maximum for the untreated‐fiber‐based composite (27%), whereas the ultrasound‐ and silane‐treated‐fiber‐based composites showed a minimum value of 8%. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42784.