Short sisal fiber‐reinforced tire rubber composites: Dynamic and mechanical properties

The world tendency toward using recycled materials demands new products from vegetable resources and waste polymers. In this work, composites made from powdered tire rubber (average particle size: 320 μm) and sisal fiber were prepared by hot‐press molding and investigated by means of dynamic mechanical thermal analysis and tensile properties. The effects of fiber length and content, chemical treatments, and temperature on dynamic mechanical and tensile properties of such composites were studied. The results showed that mercerization/acetylation treatment of the fibers improves composite performance. Under the conditions investigated the optimum fiber length obtained for the tire rubber matrix was 10 mm. Storage and loss moduli both increased with increasing fiber content. The results of this study are encouraging, demonstrating that the use of tire rubber and sisal fiber in composites offers promising potential for nonstructural applications. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 670–677, 2004     

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     

棉籽蛋白/剑麻纤维复合材料加工、界面与性能

为了提高植物蛋白基绿色高分子材料的力学性能和热稳定性能,以棉籽蛋白（CP）为原料,在尿素变性、甘油增塑、双醛淀粉（DAS）交联的基础上,将其与取向排列的天然剑麻长纤维（SF）复合,经热压硫化加工制备得到具有优异性能的棉籽蛋白/剑麻纤维全绿色复合材料。微观结构形貌和性能分析测试表明,复合材料获得改善性能主要归功于：CP基体与SF增强相间形成的紧密界面结合、对剑麻长纤维的预浸渍处理、CP与SF生物大分子间的强氢键作用。考察了不同DAS含量对复合材料力学性能和热稳定性能的影响。拉伸、热重和差示量热分析表明,经20%（质量） DAS交联的复合材料具有最优的拉伸强度（断裂应力7.5 MPa）、模量（杨氏模量93 MPa）、热稳定性（最大分解温度328℃）和玻璃化转变温度（102℃）。     

Thermal and mechanical properties of liquid silicone rubber composites filled with functionalized graphene oxide

To improve the thermal and mechanical properties of liquid silicone rubber (LSR) for application, the graphene oxide (GO) was proposed to reinforce the LSR. The GO was functionalized with triethoxyvinylsilane (TEVS) by dehydration reaction to improve the dispersion and compatibility in the matrix. The structure of the functionalized graphene oxide (TEVS‐GO) was evaluated by Thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectra, X‐ray diffraction (XRD), and energy dispersive X‐ray spectroscopy (EDX). It was found that the TEVS was successfully grafted on the surface of GO. The TEVS‐GO/LSR composites were prepared via in situ polymerization. The structure of the composites was verified by FTIR, XRD, and scanning electron microscopy (SEM). The thermal properties of the composites were characterized by TGA and thermal conductivity. The results showed that the 10% weight loss temperature (T₁₀) increased 16.0°C with only 0.3 wt % addition of TEVS‐GO and the thermal conductivity possessed a two‐fold increase, compared to the pure LSR. Furthermore, the mechanical properties were studied and results revealed that the TEVS‐GO/LSR composites with 0.3 wt % TEVS‐GO displayed a 2.3‐fold increase in tensile strength, a 2.79‐fold enhancement in tear strength, and a 1.97‐fold reinforcement in shear strength compared with the neat LSR. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42582.     

Preparation and characterization of poly(vinyl chloride)/virgin and treated sisal fiber composites

Mechanical property changes, thermal stability, and water absorption capacity of poly(vinyl chloride) (PVC)/sisal fiber composites were assessed with respect to the effect of maleic anhydride chemical treatments of the sisal fiber, for five different sisal fiber contents, varying from 0 to 30% by weight in the composite. The composites prepared with the untreated sisal exhibited higher tensile modulus and hardness than the unloaded resin, while elongation and tensile strength were reduced. The deterioration in the mechanical properties of PVC blended with sisal fiber is attributed to the presence of moisture, interfacial defects at the fiber and polymer interface, and fiber dispersion in the PVC matrix. The amount of absorbed water is a function of the amount of fiber in the composite (F0 = 0 phr, F5 = 0.77 phr, and F20 = 4.83 phr). The comparison of the results of characterization of F5, F20, and F30 formulations prepared with the untreated fibers and the treated ones showed a reduction in absorbed water after the chemical treatment of fiber with maleic anhydride (F0 = 0 phr, F5 = 0.28 phr, and F20 = 2.99 phr), thus improving the mechanical properties of composites prepared with the treated sisal. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3630–3636, 2007     

Foam processability of polypropylene/sisal fiber composites having near-critical fiber length for acoustic absorption properties

The current research aims to develop a sound-absorbing material from polypropylene (PP) and sisal fibers (SFs). The study explores the foam processability of PP/SF composites with near-critical fiber length, employing supercritical CO₂-assisted batch foaming technology. Optimized foam processing conditions were determined to be 145°C, 100 bar, and 15 min saturation time. These conditions resulted in foams with the lowest density, maximum volume expansion ratio and an overall microcellular structure. Notably, increasing the fiber concentration significantly enhanced the compressive properties, exhibiting a remarkable 3000% improvement with the addition of 40 wt% SFs. Dynamic mechanical analysis further revealed improved dampening properties of the composites after foaming. Moreover, the incorporation of SFs led to an increase in the noise reduction coefficient, while foaming additionally improved the sound absorption properties. This renders the material highly applicable for soundproofing purposes. Thus, produced PP/SF microcellular foams offer properties that can potentially be used to produce lightweight structural components for acoustic absorption applications.     

Morphology and mechanical properties of PVC/straw‐fiber coated with liquid nitrile‐butadiene rubber composites

This study exhibited an approach of high‐value utilization of straw fiber (SF) in polymer composites. The rigid poly(vinyl chloride) [PVC]/SF and PVC/SF coated with liquid nitrile‐butadiene rubber (PVC/LNBR‐SF) composites were both fabricated by melt mixing. The chemical structure and crystal structure of LNBR‐SF were characterized by Fourier Transform Infrared Spectroscopy (FTIR) and X‐ray diffraction (XRD). The mechanical properties and micro‐structure of PVC/SF and PVC/LNBR‐SF composites were also studied. FTIR and XRD results showed that the chemical structure and crystal structure of SF did not change after modifying with LNBR. The mechanical properties analysis showed that the PVC/LNBR‐SF composites exhibited better tensile strength, elongation at break and notched impact strength than those of PVC/SF composites owing to the compatibilization and toughening effect of LNBR. Scanning electron microscope results indicated that the LNBR improved the dispersion of SF in PVC matrix to some extent. The interface adhesion between SF and PVC matrix with adding LNBR was also enhanced. These results suggested that PVC/LNBR‐SF composites exhibited promising potential for practical application in substitute for wood. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44119.     

Morphology and properties of polystyrene/agave fiber composites and foams

In this work, agave fibers were blended with polystyrene to produce foamed and unfoamed composites. The effect of fiber size and density reduction on the morphological, thermal, mechanical, and rheological properties, as well as crystallinity and water absorption kinetics of the composites was assessed. The results show that Young's modulus and tensile strength increased with increasing fiber content, but decreased with density reduction. Increasing fiber content and decreasing the size of the fibers both increased crystallinity of the composites. Finally, water uptake and diffusion coefficient were found to increase with increasing fiber content for all sizes. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Effect of fiber treatment on the mechanical properties of LDPE-henequen cellulosic fiber composites

The degree of mechanical reinforcement that could be obtained by the introduction of henequen cellulosic fibers in a low-density polyethylene, LDPE, matrix was assessed experimentally. Composite materials of LDPE-henequen cellulosic fibers were prepared by mechanical mixing. The concentration of randomly oriented fibers in the composite ranged between 0 and 30% by volume. The tensile strength of these composite materials increased up to 50% compared to that of LDPE. There is also a noticeable increase in Young's modulus for the composite materials that compares favorably with that of LDPE. As expected, the addition of the fibers decreases the ultimate strain values for the composite materials. The thermal behavior of the LDPE-henequen cellulosic fibers materials, studied by differential scanning calorimetry, DSC, showed that the presence of the fibers does not affect the thermal behavior of the LDPE matrix; thus, the interaction between fiber and matrix is probably not very intimate. Preimpregnation of the cellulosic fibers in a LDPE-xylene solution and the use of a silane coupling agent results in a small increment in the mechanical properties of the composites, which is attributed to an improvement in the interface between the fibers and the matrix. The shear properties of the composites also increased with increasing fiber content and fiber surface treatment. It was also noted that the fiber surface treatment improves fiber dispersion in the matrix. © 1997 John Wiley & Sons, Inc. J Appl Polym Sci 65: 197–207, 1997     

Enhanced interfacial strength and mechanical properties of carbon fiber composites by introducing functionalized silica nanoparticles into the interface

Introducing nanoparticles onto the surface of carbon fibers (CFs) is a useful method for enhancing the quality of fiber-matrix interface. In this work, a liquid sizing agent containing functionalized silica nanoparticles (SiO₂) was well prepared to improve interfacial strength and mechanical properties of composites. In order to enhance the dispersion of SiO₂ nanoparticles in sizing agent, SiO₂ nanoparticles were chemically grafted with 3-aminopropyltriethoxysilane (APS), and then silanized silica (SiO₂-APS) was introduced into the interphase by a conventional sizing process as well. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA) confirmed the successful preparation of SiO₂-APS. Scanning electron microscopy (SEM) showed that a uniform distribution of SiO₂-APS on the fiber surface and the increased surface roughness. The sized fibers (CF/SiO₂-APS) exhibited a high surface free energy and good wettability based on a dynamic contact angle testing. Interfacial microstructure and mechanical properties of untreated and sized CFs composites were investigated. Simultaneous enhancements of interlaminar shear strength (ILSS) and impact toughness of CF/SiO₂-APS composites were achieved, increasing 44.79% in ILSS and 31.53% in impact toughness compared to those of untreated composites. Moreover, flexural strength and modulus of composites increased by 32.22 and 50.0% according to flexural test. In addition, the hydrothermal aging resistance of CF/SiO₂-APS composites has been improved significantly owing to the introduced Si-O-Si bonds at the interface.     

Study on the mechanical properties and microstructure of high-performance carbon fiber/epoxy composites

A high-toughness epoxy has been prepared using carboxyl-terminated butadiene acrylonitrile (CTBN) as a toughening agent to modify the AG-80 epoxy resin. High-performance carbon fiber/epoxy (CF/EP) composites are fabricated using the CTBN-toughened epoxy resin as the matrix and two types of CF, namely, T800SC and T800HB, as reinforcement. The mechanical properties of the matrix, surface properties of the CFs, tensile properties, and fracture morphologies of the composites are systematically investigated to elucidate the key factors influencing interfacial bonding in high-performance CF/EP composites. The results reveal that the most significant improvement in toughness is achieved when the CTBN content is 6.90 wt.% in the epoxy resin. Owing to the high content of polar functional groups and excellent surface wettability of T800SC, the T800SC/EP composite exhibits superior mechanical properties compared with the T800HB/EP composite.     

The effect of paraffin on fiber dispersion and mechanical properties of polyolefin–sawdust composites

This article reports on the influence of the paraffin (PAR) on the wood fiber (WF) dispersion in different polyethylene (low‐density polyethylene, high‐density polyethylene, recycled polyethylene) matrices, as well as on the melt flow behavior and mechanical properties of WF‐reinforced polyethylene (PE) composites. In the presence of paraffin, the composites showed improved tensile and flexural strength and modulus, but lower impact strength and elongation at break. The extent of improvement in mechanical properties depends on paraffin content and type of polyethylene; the most effective paraffin was in LDPE‐based composites. Paraffin‐treated WF showed lower moisture absorption ability in comparison with unmodified wood fiber. The phase segregation process was investigated for PE/PAR blends by DSC method. It was shown that an increase of paraffin concentration in the PE/PAR blend leads to a decrease of PE melting temperature and an increase of paraffin melting temperature; it indicates a net exchange of material from paraffin towards polyethylene. However, generally both components of PE/PAR blends remain immiscible. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2385–2393, 2004     

Thermal and mechanical properties of woodflour/tannin adhesive composites

Composite materials formulated with a natural polyphenolic matrix (commercial tannin adhesive made from quebracho tannin extract), pine woodflour as reinforcing material, and hexamethylenetetramine as hardener were prepared and tested. Scanning electron microscopy of fractured samples was used to analyze the efficiency of the wetting and adhesion of the filler to the surrounding matrix. Thermogravimetric analysis was used in the thermal characterization of the woodflour and the tannin extract. Flexural, compression, and dynamic‐mechanical tests were performed on composites to study the relationship of the filler content and particle size with the composite final properties. Moreover, the influence of the moisture content on the physical and mechanical properties of the different composites was analyzed. Results indicated that the mechanical properties were severely affected by the absorbed moisture. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3074–3082, 2004     

表面处理对剑麻纤维布/不饱和树脂材料性能影响

采用碱、高锰酸钾及热对剑麻纤维布进行了表面处理,并由真空辅助树脂传递模塑成型(VARTM)工艺制备了剑麻纤维布增强不饱和聚酯树脂复合材料。通过对复合材料的力学性能及吸水性的测试,研究了不同剑麻纤维布表面处理对其不饱和聚酯树脂复合材料性能的影响。结果表明:经过碱处理,复合材料的拉伸、弯曲,冲击强度提高最大,可分别提高26.5%,16.5%和22.6%,吸水率降低了47.5%。对剑麻纤维布进行表面处理可使复合材料的界面性能得到改善,力学性能提高,吸水性降低。     

Bamboo fiber reinforced polypropylene composites and their mechanical,thermal, and morphological properties

Short bamboo fiber reinforced polypropylene composites were prepared by incorporation of various loadings of chemically modified bamboo fibers. Maleic anhydride grafted polypropylene (MA‐g‐PP) was used as compatibilizer to improve fiber–matrix adhesion. The effects of bamboo fiber loading and modification of the resin on the physical, mechanical, thermal, and morphological properties of the bamboo reinforced modified PP composites were studied. Scanning electron microscopy studies of the composites were carried out on the interface and fractured surfaces. Thermogravimetric analysis and IR spectroscopy were also carried out. At 50% volume fraction of the extracted bamboo fiber in the composites, considerable increase in mechanical properties like impact, flexural, tensile, and thermal behavior like heat deflection temperature were observed. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Electrical conductivity and electromagnetic interference shielding effectiveness of carbon black/sisal fiber/polyamide/polypropylene composites

The effects of hybrid fillers on the electrical conductivity and electromagnetic interference (EMI) shielding effectiveness (SE) of polyamide 6 (PA6)/polypropylene (PP) immiscible polymer blends were investigated. Carbon black (CB) and steam exploded sisal fiber (SF) were used as fillers. CB was coated on the surface of SF, and this was exploded by water steam to form carbon black modified sisal fiber (CBMSF). CB/SF/PA6/PP composites were prepared by melt compounding, and its electromagnetic SE was tested in low‐frequency and high‐frequency ranges. We observed that SF greatly contributed to the effective decrease in the percolation threshold of CB in the PA6/PP matrix and adsorbed carbon particles to form a conductive network. Furthermore, an appropriate CB/SF ratio was important for achieving the best shielding performance. The results indicate that CBMSF was suitable for use as electronic conductive fillers and the CB/SF/PA6/PP composites could be used for the purpose of EMI shielding. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42801.     

Mechanical and viscoelastic properties of short fiber reinforced natural rubber composites: effects of interfacial adhesion,fiber loading,and orientation

The effect of a two-component dry bonding system consisting of resorcinol and hexamethylene tetramine on the mechanical and viscoelastic properties of short sisal fiber reinforced natural rubber composites has been studied. The studies were conducted with chemically treated and untreated short sisal fibers. Treated fibers impart better mechanical properties to the composites. By mixing with short fibers, the dynamic storage modulus (E') of natural rubber composites was improved. The effects of fiber-matrix adhesion on the mechanical and viscoelastic properties of the composites were investigated. The storage moduli and mechanical loss increased continuously with an increase in fiber loading but decreased with an increase of temperature. The influence of the fiber orientation on the mechanical and viscoelastic properties is discussed.     

Preparation,characterization, and biodegradability of renewable resource‐based composites from recycled polylactide bioplastic and sisal fibers

The biodegradability, morphology, and mechanical thermal properties of composite materials composed of polylactide (PLA) and sisal fibers (SFs) were evaluated. Composites containing acrylic acid‐grafted PLA (PLA‐g‐AA/SF) exhibited noticeably superior mechanical properties because of greater compatibility between the two components. The dispersion of SF in the PLA‐g‐AA matrix was highly homogeneous as a result of ester formation and the consequent creation of branched and crosslinked macromolecules between the carboxyl groups of PLA‐g‐AA and hydroxyl groups in SF. Furthermore, with a lower melt temperature, the PLA‐g‐AA/SF composite is more readily processed than PLA/SF. Both composites were buried in soil to assess biodegradability. Both the PLA and the PLA‐g‐AA/SF composite films were eventually completely degraded, and severe disruption of film structure was observed after 6–10 weeks of incubation. Although the degree of weight loss after burial indicated that both materials were biodegradable even with high levels of SF, the higher water resistance of PLA‐g‐AA/SF films indicates that they were more biodegradable than those made of PLA. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Influence of varying fiber lengths on mechanical,thermal, and morphological properties of MA‐g‐PP compatibilized and chemically modified short pineapple leaf fiber reinforced polypropylene composites

Environmentally benign, low cost and abundantly available short pineapple leaf fibers (PALF), found mostly in the Tropical rain forest climates are ideal materials for manufacture of thermoplastic polymer‐matrix composites. Here, mechanical and thermal properties of composites of maleic anhydride grafted polypropylene (MA‐g‐PP) and chemically modified short PALF are studied as a function of different fiber lengths at 10 vol % fibers loading with fiber orientation in the longitudinal direction. The effects of fiber lengths and fiber loading on the morphological properties are assessed via observations by scanning electron microscopy. Fiber length of 6 mm oriented longitudinally at 10 vol % fibers loading in PP is the optimum and recommended composition, where 73% increase in impact properties, 37% increase in the flexural modulus, 33% increase in flexural strength, and 14% increase in vicat softening temperature are observed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Thermal and mechanical properties of polypropylene/wood‐flour composites

In this research, polypropylene/wood‐flour composites (WPCs) were blended with different contents of wood and/or maleated polypropylene (MAPP) and clay. We found that the addition of MAPP or clay in the formulation greatly improved the dispersion of the wood fibers in the composite; this suggested that MAPP or clay may have played the role of an adhesion promoter in the WPCs. The results obtained with clay indicate that it also acted as a flame retardant. The thermal tests carried out with the produced samples showed an increased crystallization temperature (T_c), crystallinity, and melting temperature (T_m) with wood loading. The increase of the two former parameters was explained by the incorporation of wood flour, which played the role of nucleating agent and induced the crystallization of the matrix polymer. On the other hand, the T_m increase was ascribed to the insulating properties of wood, which hindered the movement of heat conduction. The effects of UV irradiation on T_m and T_c were also examined. T_c increased with UV exposure time; this implied that UV degradation generated short chains with low molecular weight that could move easily in the bulk of the sample and, thus, catalyze early crystallization. The flexural strength and modulus increased with increasing wood‐flour content. In contrast, the impact strength and tensile strength and strain decreased with increasing wood‐flour content. All of these changes were related to the level of dispersion of the wood flour in the polymeric matrix. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011