Mechanical properties of recycled kenaf/polyethylene terephthalate (PET) fiber reinforced polyoxymethylene (POM) hybrid composite

Environmental concerns have attracted researchers to study the recycling of composite materials and thermoplastics due to the desire not to waste materials and reduce disposal of scraps that may eventually pollute the environment. The main objective of this article is to study the effect of recycling on the mechanical properties of kenaf fiber/PET reinforced POM hybrid composite. The virgin hybrid composite was produced by compression molding and later subjected to mechanical testing. The scraps obtained after the mechanical testing were shredded, granulated and subjected to compression molding to produce samples for mechanical testing. Tensile strength of 27 MPa was obtained and (after second recycling process) which is lower compared to 73.8 MPa obtained for the virgin hybrid composite. There was a significant increase in flexural modulus (4.7 GPa) compared to the virgin hybrid composite. The impact strength dropped to 4.3 J cm^?1 as against 10.5 J cm^?1 for the virgin hybrid composite. The results of thermal degradation showed about 80% weight loss for kenaf fiber between 300 and 350°C. The weight loss may be due to the degradation of cellulose and hemicellulose content of the fiber. The percentage water absorption of the recycled composite dropped by about 80% compared to the virgin hybrid composite. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39831.     

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.     

Characteristics of murta bast fiber reinforced epoxy composites

The growing global concern over environment protection has led to the application of natural fiber reinforced polymer composites as alternative materials in manufacturing sectors. Various natural fibers are therefore being explored for reinforcement of polymer matrices. In the present work, murta bast fibers of varying length and weight percent are mixed randomly with the epoxy matrix and the composites are prepared from these mixtures by using the hand lay‐up method. The composites are characterized on the basis of density, thermal gravimetric analysis, infrared spectroscopy, scanning electron microscopy, tensile strength, flexural strength, compressive strength, impact strength, and Rockwell hardness studies. Tensile, flexural, and compressive moduli of the composites are also determined. The tensile strength of the composite was analyzed in the light of the different analytical models. Composites containing 30 weight % fibers of length 25 or 35 mm have the optimum mechanical properties. Murta bast fiber has the characteristics to become a good natural material for reinforcement. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44142.     

Thermal behavior of vinyl ester resin matrix composites reinforced with alkali‐treated jute fibers

The thermal behavior of vinyl ester resin matrix composites reinforced with jute fibers treated for 2, 4, 6, and 8 h with 5% NaOH was studied with Thermo‐gravimetric analysis and differential scanning calorimetry. The moisture desorption peak shifted to a higher temperature, from 37 to 58.3°C, for all the treated‐fiber composites because of improved wetting of the fibers by the resin and stronger bonding at the interface. The degradation temperature of the vinyl ester resin in the composites was lowered to 410.3°C from that of the neat resin, 418.8°C. The X‐ray diffraction studies showed increased crystallinity of the treated fibers, which affected the enthalpy of the α‐cellulose and hemicellulose degradation. The hemicellulose degradation temperature remained the same (299.7°C) in all the treated‐fiber composites, but the enthalpy associated with the hemicellulose degradation showed an increasing trend in the treated composites with a small increase in the weight loss. This could be attributed to the increased hydrogen bonding between the more accessible ? OH groups of the hemicellulose in the noncrystalline region of the jute fiber and the resin. The degradation temperature of α‐cellulose was lowered from 364.2 to 356.8°C in the treated composites. The enthalpy of α‐cellulose degradation showed a decreasing trend with a lowering of the weight loss. The crystalline regions of the fiber, consisting of closely packed α‐cellulose chains, were bonded with the resin mainly on the surface through hydrogen bonds and became more resistant to thermal degradation; this reduced the weight loss. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 123–129, 2004     

Thermal degradation of epoxy resin reinforced with polypropylene fibers

The influence of polypropylene fibers on the thermal degradation of epoxy composites was investigated with thermogravimetric analysis. Three composites with 5, 10, or 15 wt % polypropylene fibers were prepared with epoxy as a matrix material. The polypropylene fibers, used as reinforcing materials, retarded the thermal decomposition, and increasing the weight percentage of the fiber material increased the thermal stability to a certain extent. Of the three composites, the 10 wt % polypropylene fiber/epoxy resin composite showed very good thermal stability, which was indicated by the increase in the resin decomposition temperature from 280°C for the 5 wt % polypropylene fiber/epoxy resin composite to 375°C for the 10 wt % polypropylene fiber/epoxy resin composite. The Horowitz–Metzger method was used to calculate the activation energies, and the results were tabulated. A morphological analysis was carried out with scanning electron microscopy to evaluate the dispersion of the fibers in the epoxy matrix. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 500–503, 2007     

Investigation of the thermostability of poly(ethylene terephthalate)–hemp fiber composites: Extending natural fiber reinforcements to high‐melting thermoplastics

The thermal stability of poly(ethylene terephthalate) reinforced with 1, 5, 10, 15, and 20% hemp fibers was investigated with the aim of extending the applications of biocomposites to high‐melting thermoplastics. The material was injection‐molded following compounding with a torque‐based Rheomix at 240, 250, and 260°C. A combination of thermogravimetric methods at 5, 10, and 20°C/min, Liu and Yu's collecting temperature method, and Friedman's kinetic method were used for testing and analysis. A significant thermostability for all formulations was observed below 300°C; this demonstrated their potential for successful melt processing. Moreover, two degradation steps were observed in the temperature ranges 313–390 and 390–490°C. The associated apparent activation energies within the temperature ranges were determined as 150–262 and 182–242 kJ/mol, respectively. We found that the thermostability was significantly affected by the heating rates; however, the effect of the temperature of the mixing chamber was negligible. These findings suggest that the successful melt processing of high‐melting thermoplastics reinforced with natural fibers is possible with limited fiber thermodegradation. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42500.     

Characterization of an alkali‐treated grass fiber by thermogravimetric and X‐ray crystallographic analysis

The thermal behavior of grass fiber was characterized by means of thermogravimetric analysis and differential scanning calorimetry analysis. The results proved that the removal of water‐soluble matter improved the thermal behavior of grass fiber over that of unleached fiber, and this was further enhanced by an alkali treatment of the grass fiber. The isothermal weight loss of the grass‐fiber specimens was analyzed at 100, 200, and 300°C for different time periods. Accelerated aging of the grass‐fiber samples was carried out to determine the effect of aging on the tensile strength. Partially delignified grass fiber showed maximum thermal stability. X‐ray diffraction analysis was also performed to verify the composition and to correlate the change in the tensile strength due to the water leaching and alkali treatment. The processing of grass fiber with NaOH and NaClO₂ reduced the amorphous fraction in the fiber sample. This may have been a result of the loss of the amorphous noncellulosic components of the fibers and the degradation of the unordered regions of the grass fiber. However, mercerization of the grass fiber revealed an increase in the amorphous fraction after a certain time exposure, confirming the decrease in the crystallinity. The morphology of the water‐leached and alkali‐treated grass fiber was studied with scanning electron microscopy © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

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.     

Characterization of composites based on recycled expanded polystyrene reinforced with curaua fibers

This study evaluated the mechanical, thermal, rheological, and morphological properties of virgin and recycled matrices and their composites with 20 wt % of curaua fiber. The recycling process of postconsumer polystyrene was carried out by grinding and extrusion. It was found that the recycling of expanded polystyrene did not have a major influence on the mechanical properties; however, the thermal stability was increased. The addition of curaua fibers led to increases in the tensile strength, modulus of elasticity, rigidity, thermal stability and melt viscosity of the composites. The composites made with the recycled matrix revealed higher thermal stability and melt viscosity than those made with the virgin matrix. Scanning electron microscopy characterization showed empty spaces where the curaua fibers had pulled out of the matrices in the fractured regions, indicating poor interfacial adhesion without the use of a coupling agent. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

The flame retardant and thermal performances of polypropylene with a novel intumescent flame retardant

A novel mono-component intumescent flame retardant(m-IFR), called poly-(spirocyclic pentaerythritol bisphosphonate-1,3,5-triazine-O-bicyclic pentaerythritol phosphate) (PSTBP) was synthesized and characterized. PSTBP was used in polypropylene (PP) to obtain PP/PSTBP mixture whose flame retardancy, thermostability, and water resistance were studied by limiting oxygen index (LOI), vertical burning test (UL-94 V) and thermogravimetric analysis (TGA). In addition, flame-retardant mechanism of the PSTBP was investigated. The results showed that the residue of PSTBP reached 34.58% at 800°C and the volume of the PSTBP increased by dozens of times. When the content of PSTBP was 30.0 wt%, the PP/PSTBP mixture could achieve an LOI value of 32.5% and an UL-94 V-0 rating. Compared with PP/APP/PER system, PP/PSTBP mixture showed better water resistance. The TGA and Fourier transform infrared spectroscopy (FTIR) results showed that PSTBP could generate free radicals and capture the free radicals of the thermal decomposition of PP, and form a dense, strong, and thick intumescent char on the substrate, thus effectively retard the degradation and combustion of PP.     

Synthesis of restorative microcapsules having vinyl ester healing medicine for hybrid resin/modified carbon fiber self-healing composites

In this study, we aimed to synthesize restorative microcapsules using aminopropyl triethoxy silane through a combination of both microemulsions with a sol–gel technique and vinyl ester resin used as a healing component. The characteristic features of the microcapsules were analyzed by FTIR, XRD, and SEM and confirmed by the formation of core-shell microspheres with desired properties. The fabricated core-shell microspheres were reinforced into a hybrid resin (vinyl ester (80): epoxy (20)/silane modified carbon fiber composites) using the hand lay-up method. The effect of the microspheres on the mechanical and self-healing properties of composites was investigated. The mechanical test results showed a significant improvement in the flexural and impact strength by approximately 23% and 30%, respectively. The healing property was observed using the flexural test and the results indicated that the recovered strength almost 74% of the composites after initial damage was due to the healing medicine released from the broken portion of the core-shell microspheres that filled and cured the cracked area of the composites.     

炭纤维增强复合材料振动性能研究进展

炭纤维增强复合材料的固有频率和阻尼特性受复合材料的组织结构和使用环境的影响。针对炭纤维增强树脂基和炭基复合材料的固有频率和阻尼特性的研究进展进行了系统论述,详细介绍了纤维、基体、纤维/基体的界面及温度对炭纤维增强树脂基和炭基复合材料固有频率和阻尼特性的影响。     

Compositional analysis of thermoplastic wood composites by TGA

A method has been developed for the quantitative determination of the composition of thermoplastic wood composites. The method involves area measurements of the two peaks in the derivative curve of a tracing produced by the thermogravimetric analysis (TGA) of a thermoplastic composites sample in an inert atmosphere. This may involve the standard, constant heating rate method or the high resolution (Hi‐Res?) TGA method; both produce virtual baseline separation between wood and polyolefin peaks over a wide compositional range. Because this baseline separation suffers from a mutual effect on the thermal degradation of wood and polyolefins, best results are obtained if the parameters relating peak area with polyolefin content are different below and above 40% polyolefin content. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1484–1492, 2004     

Surface treatment of cellulose fibers with methylmethacrylate for enhanced properties of in situ polymerized PMMA/cellulose composites

Cellulose micro/nanofibers (CNF), prepared from jute fibers were surface treated with methyl methacrylate (MMA) for better dispersion into poly methyl methacrylate (PMMA) matrix. PMMA/cellulose composites were prepared by in situ suspension polymerization technique. The surface treatment of CNF was confirmed by Fourier transform infrared spectroscopy (FTIR) and Nuclear magnetic resonance (NMR) analysis. MMA‐treated cellulose micro/nanofibers (MCNF) demonstrated improved affinity and dispersion in MMA monomer as well as in the PMMA/cellulose composites. Thermal properties of the cellulose composites were analyzed by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The glass transition temperature (T_g) of PMMA increased by nearly 19°C in the in situ cellulose composites compared to that of unreinforced PMMA as indicated by DSC. TGA showed increased thermal stability of the cellulose composites. Enhanced tensile properties as well as significantly lower moisture uptake were observed in the in situ prepared PMMA/cellulose composites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39808.     

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     

Multiscale thermal study of virgin and aged polyphenylene sulfide reinforced by glass fiber

In this study, virgin and thermal aged PPS samples were prepared and tested using different techniques such as thermogravimetric analysis (TGA), coupled TGA–Fourier transform infrared spectroscopy (FTIR), and FTIR as well as optical microscopy. Some interesting research results can be summarized as follows: TGA results prove the PPS composite samples aged at 180 and 200°C have been degraded obviously during the aging period in oven. Moreover, accelerated aging leads to the degradation of PPS composite with the observation of increased thermal oxidation layer from outside to inside. There is a plateau standing at about 350 μm for the thermal oxidation layer at oxidation temperature of 200°C. Some thermal decomposition models are applied to clarify the degradation kinetics of PPS composite. According to the activation energy value, it appears degradation more easily at the beginning of the heating process in the atmosphere of oxygen than that of nitrogen. Moreover, the related products of PPS composites during pyrolysis are fully discussed with the combined analysis of TGA–FTIR techniques.     

Interfacial,dynamic mechanical,and thermal fiber reinforced behavior of MAPE treated sisal fiber reinforced HDPE composites

The present article summarizes an experimental study on the mechanical and dynamic mechanical behavior of sisal fiber reinforced HDPE composites. Variations in mechanical strength, storage modulus (E′), loss modulus (E″), and damping parameter (tan δ) with the addition of fibers and coupling agents were investigated. It was observed that the tensile, flexural, and impact strengths increased with the increase in fiber loading up to 30%, above which there was a significant deterioration in the mechanical strength. Further, the composites treated with MAPE showed improved properties in comparison with the untreated composites. Dynamic mechanical analysis data also showed an increase in the storage modulus of the treated composites The tan δ spectra presented a strong influence of fiber content and coupling agent on the α and γ relaxation process of HDPE. The thermal behavior of the composites was evaluated from TGA/DTG thermograms. The fiber–matrix morphology in the treated composites was confirmed by SEM analysis of the tensile fractured specimens. FTIR spectra of the treated and untreated composites were also studied, to ascertain the existence of type of interfacial bonds. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3306–3315, 2006     

Effect of maleated polypropylene as coupling agent for polypropylene composites reinforced with hemp strands

New composites based on poly(propylene) as polymer matrix and hemp strands as natural reinforcement have been developed by injection‐molding. The materials were previously mixed in a two roll mill to induce the dispersion of the fiber inside the polymer. To improve the adhesion between both components, maleated poly(propylene) was added as coupling agent, at 4% wt/wt with respect to hemp strands. The addition of this amount of this coupling agent to the formulation modified with 40 wt % of hemp strands increases the ultimate tensile strength (σ_t) and flexural strength (σ_f) up to 49 and 38%, respectively, compared with the composite without coupling agent. The interaction between the surface of hemp strands and the coupling agent was determined by FT‐IR spectroscopy assuming that a covalent bond was established, avoiding the adverse effect of the poor compatibility at the interface for this kind of composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 833–840, 2006     

Evaluating the thermal stability of high performance fibers by TGA

The thermal degradation of eight types of high performance fibers (HPFs) was measured under nitrogen and air atmosphere. The degree of degradation, as measured by weight loss using thermogravimetric analysis (TGA), and the characteristic degradation temperatures were obtained. The kinetics of the thermal degradation has also been analyzed according to the Freeman–carroll method and the activation energies of the HPFs were estimated. The experimental results show that para‐aramids (Kevlar® 29, 49, 129, and Twaron®2000) have similar thermal stability, but their thermal degradation temperatures and activation energies in air are different from those in nitrogen, which means that the thermostability of the fiber depends not only on its intrinsic structure but also on the atmosphere and temperature of testing environment. Terlon® fiber shows higher degradation temperature as a copolymer of para‐aramid, and its initial degradation temperature is 476.4°C in air. It can also be found that the PBO (poly(p‐phenylene benzobisoxazole)) fiber has the highest thermal degradation temperature among the samples tested, but its activation energy is not the highest in both air and nitrogen atmosphere. And the UHMW‐PE (ultra high molecular weight polyethylene) fiber has the lowest thermal degradation temperature, and it begins to degrade when the temperature reaches 321.8°C under air atmosphere. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 937–944, 2006     

Thermal,mechanical, and dielectric properties of aluminum silicate fiber reinforced aluminum phosphate–poly(ether sulfone) layered composites

In this study, a novel aluminum phosphate (AlPO₄) heat‐resistant layer reinforced with aluminum silicate fiber (ASF) was successfully compounded on a poly(ether sulfone) (PES) matrix via the preparation process of high‐temperature heat treatment and vacuum hot‐pressing sintering technique. The influence of the ASF content on the morphology, thermal, mechanical, and dielectric properties of the as‐fabricated aluminum silicate fiber reinforced aluminum phosphate–poly(ether sulfone) (ASF/AlPO₄–PES) layered composite was investigated. The results reveal that the incorporation of aluminum silicate fiber/aluminum phosphate (ASF/AlPO₄) heat‐resistant layer can significantly improve the thermal stability and mechanical performances of the PES matrix composites. Compared with the pristine PES, the ASF/AlPO₄–PES layered composite containing 8.0 wt % ASF exhibited better high‐temperature resistance properties (300 °C) and a lower thermal conductivity (0.16 W m^?1 K^?1). Furthermore, the dielectric constant and dielectric loss tangent of this PES matrix composite decreased to 2.16 and 0.007, respectively. Meanwhile, the frequency stability of the dielectric properties for the ASF/AlPO₄–PES layered composites was remarkably enhanced with increasing ASF addition at frequencies ranging from 10² Hz to 5 MHz. This was attributed to the existence of microscopic pores within the ASF/AlPO₄ layer and the strong interfacial bonding between the ASF/AlPO₄ layer and the PES matrix. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45542.