Polymerization compounding composites of nylon‐6,6/short glass fiber

Nylon‐6,6 was grafted onto the surface of short glass fibers through the sequential reaction of adipoyl chloride and hexamethylenediamine onto the fiber surface. Grafted and unsized short glass fibers (USGF) were used to prepare composites with nylon‐6,6 via melt blending. The glass fibers were found to act as nucleating agents for the nylon‐6,6 matrix. Grafted glass fiber composites have higher crystallization temperatures than USGF composites, indicating that grafted nylon‐6,6 molecules further increase crystallization rate of composites. Grafted glass fiber composites were also found to have higher tensile strength, tensile modulus, dynamic storage modulus, and melt viscosity than USGF composites. Property enhancement is attributed to improved wetting and interactions between the nylon‐6,6 matrix and the modified surface of glass fibers, which is supported by scanning electron microscopy (SEM) analysis. The glass transition (tan δ) temperatures extracted from dynamic mechanical analysis (DMA) are found to be unchanged for USGF, while in the case of grafted glass fiber, tan δ increases with increasing glass fiber contents. Moreover, the peak values (i.e., intensity) of tan δ are slightly lower for grafted glass fiber composites than for USGF composites, further indicating improved interactions between the grafted glass fibers and nylon‐6,6 matrix. The Halpin‐Tsai and modified Kelly‐Tyson models were used to predict the tensile modulus and tensile strength, respectively.     

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     

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

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

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.     

Novel eco‐friendly biodegradable coir‐polyester amide biocomposites: Fabrication and properties evaluation

Biocomposites are prepared from a cheap, renewable natural fiber, coir (coconut fiber) as reinforcement with a biodegradable polyester amide (BAK 1095) matrix. In order to have better fiber‐matrix interaction the fibers are surface modified through alkali treatment, cyanoethylation, bleaching and vinyl grafting. The effects of different fiber surface treatments and fiber amounts on the performance of resulting bio‐composites are investigated. Among all modifications, cyanoethylated coir‐BAK composites show better tensile strength (35.50 MPa) whereas 7% methyl methacrylate grafted coir‐BAK composites show significant improvement in flexural strength (87.36 MPa). The remarkable achievement of the present investigation is that a low strength coir fiber, through optimal surface modifications, on reinforcement with BAK show an encouraging level of mechanical properties. Moreover, the elongation at break of BAK polymer is considerably reduced by the incorporation of coir fibers from nearly 400% (percent elongation of pure BAK) to 16‐24% (coir‐BAK biocomposites). SEM investigations show that surface modifications improve the fiber‐matrix adhesion. From biodegradation studies we find that after 52 days of soil burial, alkali treated and bleached coir‐BAK composites show significant weight loss. More than 70% decrease in flexural strength is observed for alkali treated coir‐BAK composites after 35 days of soil burial. The loss of weight and the decrease of flexural strength of degraded composites are more or less directly related.     

Injection‐molded short hemp fiber/glass fiber‐reinforced polypropylene hybrid composites—Mechanical,water absorption and thermal properties

Natural fiber‐based thermoplastic composites are generally lower in strength performance compared to thermoset composites. However, they have the advantage of design flexibility and recycling possibilities. Hybridization with small amounts of synthetic fibers makes these natural fiber composites more suitable for technical applications such as automotive interior parts. Hemp fiber is one of the important lignocellulosic bast fiber and has been used as reinforcement for industrial applications. This study focused on the performance of injection‐molded short hemp fiber and hemp/glass fiber hybrid polypropylene composites. Results showed that hybridization with glass fiber enhanced the performance properties. A value of 101 MPa for flexural strength and 5.5 GPa for the flexural modulus is achieved from a hybrid composite containing 25 wt % of hemp and 15 wt % of glass. Notched Izod impact strength of the hybrid composites exhibited great enhancement (34%). Analysis of fiber length distribution in the composite and fracture surface was performed to study the fiber breakage and fracture mechanism. Thermal properties and resistance to water absorption properties of the hemp fiber composites were improved by hybridization with glass fibers. Overall studies indicated that the short hemp/glass fiber hybrid polypropylene composites are promising candidates for structural applications where high stiffness and thermal resistance is required. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2432–2441, 2007     

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     

Injection molded self‐hybrid composites based on polypropylene and natural fibers

Self‐hybrid thermoplastic composites (combination of two fiber sizes) were obtained by injection molding using pine or agave fibers with polypropylene (PP). The effect of self‐hybridization was determined through mechanical properties and water absorption for different total fiber contents between 10 and 30% wt. The results showed that impact strength (30% of fiber) and tensile modulus (20% of fiber) were improved by self‐hybridization compared with composites formulated with only one fiber size. Flexural properties were not improved by self‐hybridization. On the other hand, the combination of two fiber sizes had no effect on the water absorption behavior of these composites. Overall, the total fiber content was found to be an important parameter with 20% being the optimum condition where self‐hybridization provides the best mechanical properties. POLYM. COMPOS., 35:1798–1806, 2014. © 2013 Society of Plastics Engineers     

Structure–property relationships in glass‐reinforced polyamide,part 1: The effects of fiber content

We present the results of an extensive study of the performance of injection‐molded glass‐fiber reinforced polyamide 66 with glass content between 0 and 40% and based on two chopped glass products both sized with polyamide compatible sizing. Mechanical properties generally improved with increasing glass content, modulus linearly, strength with a maximum at 40–50% glass content, and impact showing an initial decrease from the resin value with a minimum at 4% glass content before increasing at higher glass contents. Residual fiber length decreased linearly with increasing glass content. Interfacial strength was found to be in the range of 30–36 MPa, and no significant differences in dry as molded performance was found between the 123D and 173X sizings. Conditioning these composites in either boiling water or water/glycol mixtures leads to a dramatic drop in both tensile modulus and tensile strength. This is most likely due to the high level of matrix plasticization. After conditioning, the 173X sized glass delivered a significantly higher level of tensile elongation at all fiber contents. Excellent agreement was obtained between the experimental data and the theoretical predictions of the rule of mixtures model for modulus and the Kelly‐Tyson model for strength over the range of fiber concentrations studied. POLYM. COMPOS. 27:552–562, 2006. © 2006 Society of Plastics Engineers     

Effects of organo‐montmorillonite on the mechanical and morphological properties of epoxy/glass fiber composites

Epoxy composites filled with glass fiber and organo‐montmorillonite (OMMT) were prepared by the hand lay‐up method. The flexural properties of the epoxy/glass fiber/OMMT composites were characterized by a three‐point bending test. The flexural modulus and strength of epoxy/glass fiber were increased significantly in the presence of OMMT. The optimum loading of OMMT in the epoxy/glass fiber composites was attained at 3 wt%, where the improvement in flexural modulus and strength was approximately 66 and 95%, respectively. The fractured surface morphology of the epoxy/glass fiber/OMMT composites was investigated using field emission scanning electron microscopy. It was found that OMMT adheres on the epoxy/glass fiber interface, and this is also supported by evidence from energy dispersive X‐ray analysis. Copyright © 2007 Society of Chemical Industry     

Study on short glass fiber‐reinforced poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) composites

Biobased non‐fossil polyester poly(3‐hydroxybutyrate‐co‐4‐hydroxybutyrate) (P3/4HB) containing 4.0 mol % 4‐hydroxybutyrate (4HB) was melt‐mixed with short glass fibers (SGF) via a co‐rotating twin‐screw extruder. The compositing conditions, average glass fiber length and distribution, thermal, crystallization, and mechanical properties of the P3/4HB/SGF composites were investigated. Calcium stearate, two kinds of paraffin wax and modified ethylene bis‐stearamide (TAF) were investigated as lubricants for the P3/4HB/SGF composites. It revealed that TAF is the most efficient lubricant of the P3/4HB/SGF composites. Coupling agents 2,2′‐(1,3‐phenylene)bis‐2‐oxazoline (1,3‐PBO) and pyromellitic dianhydride (PMDA) were used as end‐group crosslinkers to reduce the degradation of P3/4HB and increase the mechanical properties of the P3/4HB/SGF composites. It showed that 1,3‐PBO is the efficient coupling agent. The optimum condition of the P3/4HB/SGF composites is 1.5 phr TAF, 1.0 phr 1,3‐PBO, and 30 wt % glass fiber content. And the maximum of tensile strength, tensile modulus, and impact strength of the composites is 3.7, 6.6, 1.8 times of the neat P3/4HB polymer, respectively. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Short glass fiber reinforced ABS and ABS/PA6 composites: Processing and characterization

In this study acrylonitrile‐butadiene‐styrene (ABS) terpolymer was reinforced with 3‐aminopropyltrimethoxysilane (APS)‐treated short glass fibers (SGFs). The effects of SGF concentration and extrusion process conditions, such as the screw speed and barrel temperature profile, on the mechanical properties of the composites were examined. Increasing the SGF concentration in the ABS matrix from 10 wt% to 30 wt% resulted in improved tensile strength, tensile modulus and flexural modulus, but drastically lowered the strain‐at‐break and the impact strength. The average fiber length decreased when the concentration of glass fibers increased. The increase in screw speed decreased the average fiber length, and therefore the tensile strength, tensile modulus, flexural modulus, and impact strength were affected negatively and the strain‐at‐break was affected positively. The increase in extrusion temperature decreased the fiber length degradation, and therefore the tensile strength, tensile modulus, flexural modulus, and impact strength increased. At higher temperatures the ABS matrix degraded and the mechanical strength of the composites decreased. To obtain a strong interaction at the interface, polyamide‐6 (PA6) at varying concentrations was introduced into the ABS/30 wt% SGF composite. The incorporation and increasing amount of PA6 in the composites broadened the fiber length distribution (FLD) owing to the low melt viscosity of PA6. Tensile strength, tensile modulus, flexural modulus, and impact strength values increased with an increase in the PA6 content of the ABS/PA6/SGF systems due to the improved adhesion at the interface, which was confirmed by the ratio of tensile strength to flexural strength as an adhesion parameter. These results were also supported by scanning electron micrographs of the ABS/PA6/SGF composites, which exhibited an improved adhesion between the SGFs and the ABS/PA6 matrix. POLYM. COMPOS. 26:745–755, 2005. © 2005 Society of Plastics Engineers     

Mechanical properties and dynamic mechanical analysis of thermoplastic‐natural‐rubber‐reinforced short carbon fiber and kenaf fiber hybrid composites

The hybridization of thermoplastic natural rubber based on carbon fiber (CF) and kenaf fiber (KF) was investigated for its mechanical and thermal properties. Hybrid composites were fabricated with a melt‐blending method in an internal mixer. Samples with overall fiber contents of 5, 10, 15, and 20 vol % were subjected to flexural testing, and samples with up to 30% fiber content were subjected to impact testing. For flexural testing, generally, the strength and modulus increased up to 15 vol % and then declined. However, for impact testing, higher fiber contents resulted in an increment in strength in both treated and untreated composites. Thermal analysis was carried out by means of dynamic mechanical analysis on composites with 15 vol % fiber content with fractions of CF to KF of 100/0, 70/30, 50/50, 30/70, and 0/100. Generally, the storage modulus, loss modulus, and tan δ for the untreated hybrid composite were more consistent and better than those of the treated hybrid composites. The glass‐transition temperature of the treated hybrid composite was slightly lower than that of the untreated composite, which indicated poor damping properties. A scanning electron micrograph of the fracture surface of the treated hybrid composite gave insight into the damping characteristics. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Experimental investigation on the influence of the composition on the morphology and the mechanical properties of short glass fiber‐reinforced polypropylene nanocomposites

Polypropylene composites containing 0–5 wt% layered silicate and 0–30 wt% short glass fibers are prepared by melt compounding. To investigate the influence of different compositions on the mechanical properties of short glass fiber‐reinforced polypropylene nanocomposites, materials with various filler contents are prepared. At a glass fiber content of 10 wt% Young's modulus of the layered silicate‐containing composites decreases by around 30% compared to conventional glass fiber‐reinforced polypropylene. But at higher glass fiber loadings, an increasing modulus of up to 10% is observed. However, the addition of layered silicate results in large decreases of the tensile and the notched impact strength. A maleic anhydride‐grafted polypropylene enhances Young's modulus and the tensile strength. © 2012 Society of Plastics Engineers     

Impact modification of polypropylene‐based composites using surface‐coated waste rubber crumbs

Blends of maleated polypropylene (MAPP) with high contents of waste rubber powder, namely ground tire rubber and waste ethylene propylene diene monomer (EPDM) powder, were used as impact modifiers for polypropylene (PP) based composites with different reinforcements (hemp, talc, and milled glass fiber). Adding reinforcements led to increase in modulus (tensile, flexural, and torsion moduli) of PP, while its impact strength decreased noticeably. Impact modification of PP‐based composites was successfully performed via inclusion of MAPP/waste rubber compounds, especially compounds containing waste EPDM powder. Inclusion of such impact modifiers increased impact strength of composites over 80%. The effects of impact modification were more significant for hemp‐ and glass‐filled composites compared to composites containing talc. However, slight decrease in tensile, flexural, and torsion moduli (up to 30%) of the composites was also observed after inclusion of impact modifiers. POLYM. COMPOS., 35:2280–2289, 2014. © 2014 Society of Plastics Engineers     

Development and physico‐mechanical behavior of LDPE–sisal prepreg‐based composites

Low‐density polyethylene (LDPE)‐coated sisal fiber prepreg was prepared by using solution coating process. These coated fiber prepregs were consolidated to make composites having different weight fraction of sisal fibers in a hot compression‐molding machine. This experimental study reveals that higher loading of sisal fiber up to 57wt% in LDPE–sisal composites is possible by this technique. Mechanical and abrasive wear characteristics of these composites were determined. The tensile strength of composites increased with the increase in sisal fiber concentration. Coating thickness of LDPE was varied by changing the viscosity of LDPE–xylene solution that manifested to different weight fraction of fiber in sisal–LDPE composites. Mechanical, dynamic mechanical, and abrasive wear characteristics of these composites were determined. The tensile strength and modulus of sisal composites reached to 17.4 and 265 MPa, respectively, as compared to 7.1 and 33MPa of LDPE. Storage modulus of sisal composites LD57 reached to 2.7 × 10⁹ MPa at 40°C as compared to 8.1 × 10⁸ MPa of LDPE. Abrasive wear properties of LDPE and its composites were determined under multi‐pass mode; pure LDPE showed minimum specific wear rate. The specific wear rate of composites decreased with the sliding distance. Increase of coated sisal fiber content increased the specific wear rate at all the sliding distances, which has been explained on the basis of worn surface microstructures observed by using SEM. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Degradation of linear low-density polyethylene/poly(vinyl alcohol)/kenaf composites

The interest of this study was to examine various kenaf (KNF) loadings and burial time, and their effects on degradability behavior of linear low-density polyethylene/poly(vinyl alcohol)/kenaf (LLDPE/PVOH/KNF) composites in soil. The LLDPE/PVOH/KNF composites with various KNF loadings were melt-mixed in a Thermo Haake internal mixer. The composites were buried in soil and their extent of degradability was assessed by tensile properties, morphological study, and weight loss and crystallinity measurements of the degraded composites. Fourier transform infrared spectroscopy was utilized to monitor the changes in chemical structure of the composites before and after degradation in soil. The results showed that with increase in KNF loading, the tensile modulus increased; meanwhile, the tensile strength and elongation-at-break of the degraded composites were dropped. Tensile properties of the degraded composites were decreased with prolonging soil burial time. The formation of cracks and pores was observed in field emission scanning electron microscope micrographs. By measuring the weight loss in LLDPE/PVOH/KNF composite samples before and after the soil burial testing and differential scanning calorimetry measurements, it was found that the weight loss and crystallinity of the composites increased with soil burial time. The degradation of the composites was confirmed by the formation of a strong absorption band assigned to carbonyl groups.     

Novel low‐cost jute–polyester composites. III. Weathering and thermal behavior

Jute–polyester composites were fabricated with untreated (control) and bleached slivers with 60% loading of fiber by weight and were designated as JPH(C) and JPH(B), respectively. Both types of composite specimens were subjected to water absorption and outdoor weathering tests to assess their relative performance under environmental conditions. While both composites showed low water absorption, JPH(B) showed lesser water absorption (8.48%) than did JPH(C) (12.25%). The mechanical properties like tensile and flexural strengths were measured for both the weathered and unweathered specimens and compared. The tensile strength of JPH(C) and JPH(B) decreased while the tensile modulus increased after weathering. The flexural strength, moduli, and ILSS of the weathered specimens were less than those of the unweathered ones. The nature of the fiber–matrix adhesion could be established from these results. The cause of every observation is explained. Thermal analyses (TG/DTG and DSC) of the composite specimens were also done. The overall thermal stability of JPH(C) was found to be better than that of JPH(B). © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1671–1679, 2000     

Biopolyamide hybrid composites for high performance applications

This study focuses on the performance characteristics of wood/short carbon fiber hybrid biopolyamide11 (PA11) composites. The composites were produced by melt‐compounding of the fibers with the polyamide via extrusion and injection molding. The results showed that mechanical properties, such as tensile and flexural strength and modulus of the wood fiber composites were significantly higher than the PA11 and hybridization with carbon fiber further enhanced the performance properties, as well as the thermal resistance of the composites. Compared to wood fiber composites (30% wood fiber), hybridization with carbon fiber (10% wood fiber and 20% carbon fiber) increased the tensile and flexural modulus by 168% and 142%, respectively. Izod impact strength of the hybrid composites exhibited a good improvement compared to wood fiber composites. Thermal properties and resistance to water absorption of the composites were improved by hybridization with carbon fiber. In overall, the study indicated that the developed hybrid composites are promising candidates for high performance applications, where high stiffness and thermal resistance are required. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43595.     

Tribological behavior of short‐fiber‐reinforced polyimide composites under dry‐sliding and water‐lubricated conditions

Polyimide composites reinforced with short‐cut fibers such as carbon, glass, and quartz fibers were fabricated by the polymerization of monomer reactants process. The mechanical properties of the composites with different fiber contents were evaluated. The friction and wear properties of the polyimide and its composites were investigated under dry‐sliding and water‐lubricated conditions. The results indicated that the short‐carbon‐fiber‐reinforced polyimide composites had better tensile and flexural strengths and improved tribological properties in comparison with glass‐fiber‐ and quartz‐fiber‐reinforced polyimide composites. The incorporation of short carbon fibers into the polyimide contributed to decreases in the friction coefficient and wear rate under both dry and water‐lubricated conditions and especially under water lubrication because of the boundary lubrication effect of water. The polyimide and its composites were characterized by plastic deformation, microcracking, and spalling under both dry and water‐lubricated conditions, which were significantly abated under the water‐lubricated condition. The glass and quartz fibers were easily abraded and broken; the broken fibers transferred to the mating metal surface and increased the surface roughness of mating stainless steel, which led to the wear rate increasing for the glass‐fiber‐ and quartz‐fiber‐reinforced polyimide composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2008