Biodegradability and mechanical properties of agro‐flour–filled polybutylene succinate biocomposites

The objective of this study was the production of rice husk flour (RHF) and wood flour (WF) filled polybutylene succinate (PBS) biocomposites as alternatives to cellulosic material filled conventional plastic (polyolefins) composites. PBS is one of the biodegradable polymers, made from the condensation reaction of 1,4‐butanediol and succinic acid that can be naturally degraded in the natural environment. We compared the mechanical properties between conventional plastics and agro‐flour–filled PBS biocomposites. We evaluated the biodegradability and mechanical properties of agro‐flour–filled PBS biocomposites according to the content and filler particle size of agro‐flour. As the agro‐flour loading was increased, the tensile and impact strength of the biocomposites decreased. As the filler particle size decreased, the tensile strength of the biocomposites increased but the impact strength decreased. The addition of agro‐flour to PBS produced a more rapid decrease in the tensile strength, notched Izod impact strength, and percentage weight loss of the biocomposites during the natural soil burial test. These results support the application of biocomposites as environmentally friendly materials. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1513–1521, 2005     

Effect on modified nanoclay on dynamic mechanical and thermomechanical properties of natural fiber/polypropylene biocomposites

This study was conducted to investigate the effect of nanoclay addition on thermal and dynamic mechanical properties of polypropylene (PP) biocomposites reinforced with bleached red algae fiber (BRAF), kenaf fiber (KF), and cotton pulp fiber (CPF). The nano-biocomposites were fabricated with 40?wt.% loading of all natural fibers and addition of nanoclay at 5 or 10?wt.% loading by the melting compounding and compression molding techniques. The nanoclay effects on the thermal and dynamic mechanical properties of the biocomposites were analyzed as a function of properties of natural fibers such as chemical composition, fiber length, and surface morphology. Although the thermal decomposition temperature of nano-biocomposites decreased with the addition of nanoclay, the dimensional stability of biocomposites greatly improved with increasing nanoclay loading. Also, the dynamic mechanical properties of nano-biocomposites for the PP reinforced with BRAF, KF, and CPF were enhanced with the addition of 5?wt% nanoclay compared to those of biocomposites without nanoclay. The highest enhancement in dimensional stability was obtained for the nano-biocomposites reinforced with BRAF natural fiber. These increases can be attributed to a uniform distribution of nanoclay and to a good interfacial adhesion between the reinforcement and PP matrix. The well dispersed nanoclay particles can have good interactions with both natural fibers and polymer matrix, with the incorporation of the reinforcing natural fibers restricting the mobility of the polymer molecules resulting in the raised storage modulus values.     

Rheological and mechanical properties of compatibilized polystyrene/ethylene vinyl acetate blends

In this study, a blend of polystyrene (PS)/ethylene vinyl acetate (EVA) (PS/EVA, 90 : 10 wt %) was compatibilized with three different block copolymers, in which their end blocks were compatible with either styrene or EVA. The compatibilized blends with different compositions were prepared using a twin‐screw extruder and injection molded into the required test specimens. Mechanical properties of the blends, such as tensile properties and Charpy impact strength, morphology of tensile fractured surfaces, rheological properties, and thermal properties, were investigated. The results show that the interaction between the dispersed and continuous phase can be improved by the addition of a compatibilizer. Appreciable improvement in the impact strength of the blend with 15 wt % of compatibilizer C (polystyrene‐block‐polybutadiene) was observed. Its mechanical properties are comparable to those of the commercial high‐impact polystyrene, STYRON 470. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2071–2082, 2004     

Morphology and mechanical properties of PET/PE blends compatibilized by nanoclays: Effect of thermal stability of nanofiller organic modifier

Poly(ethylene terephtalate)/poly(ethylene) (PET/PE) blends (80/20 wt %) were prepared by melt‐extrusion and compatibilized by addition of nanoclays. Two commercially available organically modified montmorillonites (Cloisite© 10A and 30B) were chosen as reference and a third one was specially organomodified at lab scale with a thermally stable phosphonium surfactant using conventional cationic exchange reaction. The size of the dispersed polymer phase (PE droplets) and the ductility of the blends depend more on the thermal stability of the surfactant of the organomodified clay than on the enthalpic interactions between the blend components and the surfactants used for the modification of the clays. The highest mechanical properties (yield stress and elongation at break) and the better compatibilization efficiency (smallest dispersed PE droplets) were observed in the presence of phosphonium organomodified montmorillonite compared to other less thermally stable commercial organoclays. The analysis of the thermal stability, morphology, and mechanical properties of PET/PE blends containing the surfactants alone in the absence of clay made it possible to evidence separately the effects of the surfactant and of the nanofiller. The role of the surfactant as compatibilization agent was demonstrated. In the absence of nanofiller, the finest morphological and highest ductility were again obtained with the phosphonium surfactant which is the most thermally stable. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Polystyrene and polyether polyurethane elastomer blends compatibilized by SMA: Morphology and mechanical properties

Blends of polystyrene (PS) and the polyether polyurethane elastomer (PU‐et) were prepared by melt mixing using poly(styrene‐co‐maleic anhydride) (SMA) containing 7 wt % of maleic anhydride as a compatibilizer. The polyurethane in the blends was crosslinked using dicumyl peroxide or sulfur. The content of maleic anhydride was varied in the blends through the addition of different SMA amounts. The morphology of the blends was analyzed by SEM and a drastic reduction of both the domain size and its distribution was observed with increase of the anhydride content in the blends. The morphology of the PU‐et blends also showed dependence on the crosslinker agent used for the elastomer, and larger domains were obtained for the elastomer phase crosslinked with dicumyl peroxide. The mechanical properties of the blends were evaluated by flexural and impact strength tests. The blend containing 0.5 wt % of maleic anhydride and 20 wt % of PU‐et crosslinked with sulfur showed the highest strength impact, which was three times superior to the PS strength impact, and the blends containing 20 wt % of PU‐et crosslinked with dicumyl peroxide showed the highest deflection at break independent of the anhydride content. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 830–837, 2002     

Wood flour/polylactide biocomposites toughened with polyhydroxyalkanoates

Polylactide (PLA)‐based wood–plastic composites (WPCs) were successfully manufactured by extrusion blending followed by injection molding. The effects of polyhydroxyanoates (PHAs) on the mechanical and thermal properties and the morphologies of the PLA‐based WPCs were investigated with mechanical testing, thermal analysis, and scanning electronic microscopy (SEM). The inclusion of PHAs in the PLA‐based WPCs produced an increase in the impact resistance and a decrease in the tensile strength. The brittle–ductile transition of the impact strength for the PLA‐based WPCs toughened with PHAs was confirmed when the wood flour content was between 15 and 35 wt %. SEM images showed that the fracture surfaces of the PLA‐based WPCs toughened with PHAs were rougher than that of their nontoughened counterparts. The ternary PLA‐based WPCs exhibited ductile fracture during mechanical testing. Differential scanning calorimetry (DSC) showed that addition of PHAs into the composites caused deviations of the cold crystallization temperature and melting temperature of PLA. Thermogravimetric analysis indicated that the PHAs reduced the thermal stability of the PLA‐based WPCs. PHAs can be a green toughening agent for PLA‐based WPCs. The specific properties evidenced by the biocomposites may hint at their potential application, for example, in the automotive industry and civil engineering. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

An investigation on recycled PET/PP and recycled PET/PP‐EP compatibilized blends: Rheological,morphological, and mechanical properties

The effectiveness of P(E‐co‐MA‐co‐GMA) as a compatibilizer for recycled PET/PP and recycled PET/PP‐EP (polypropylene (ethylene‐propylene) heterophase copolymer) blends was investigated by means of morphological (scanning electron microscopy), rheological (small amplitude oscillatory shear), mechanical (tensile, flexural and impact tests), and thermal (differential scanning calorimetry) properties. Compatibilizer concentration ranged from 1 to 5 wt % with respect to the whole blend. All blends were obtained in a 90/10 composition using a twin screw extruder. Compatibilization effects for PETr/PP‐EP were more pronounced due to ethylene segments present in both PP‐EP and P(E‐co‐EA‐co‐GMA). PETr/PP‐EP has shown greater dispersed phase size reduction, a more solid‐like complex viscosity behavior and larger storage modulus at low frequencies in relation to PETr/PP blend. For both investigated blends, mechanical properties indicated an improvement in both elongation at break and impact strength with increasing compatibilizer content. PETr/PP‐EP blends showed improved performance for the same level of compatibilizer content. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41892.     

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     

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.     

An efficient way to improve the mechanical properties of polypropylene/short glass fiber composites

Enhancement of tensile strength, impact strength, and flexural strength of polypropylene/short glass fiber composites by treating the glass fibers with coupling agent, mixing with maleated polypropylene (MPP) for compatibilization and adhesion, and with nucleating agent for improvement of polypropylene crystallization was studied. The results showed that both the silane coupling agent and MPP enhance tensile strength, impact strength, and flexural strength. In the absence of MPP, the effect of silane coupling agent on the mechanical properties of the composites decreases in the following order: alkyl trimethoxy silane (WD‐10) > γ‐methacryloxypropyl trimethoxysilane (WD‐70) > N‐(β‐aminoethyl)‐γ‐aminopropyl trimethoxysilane (WD‐52), whereas in the presence of MPP, the order changes as follows: WD‐70 > WD‐10 > WD‐52. When the glass fibers were treated with WD‐52, 4,4‐diamino‐diphenylmethane bismaleimide (BMI) can further enhance the mechanical properties of the composite. The three kinds of strengths increase with MPP amount to maximum values at 5% MPP. As a nucleating agent, adipic acid is better than disodium phthalate in improving the mechanical properties, except for the notched impact strength. Wide‐angle X‐ray diffraction showed that the adipic acid is an α‐type nucleating agent, whereas disodium phthalate is a β‐type nucleating agent. Blending with styrene–butadiene rubber can somewhat improve the notched impact strength of the composites, but severely lowers the tensile strength and bending strength. Scanning electron micrographs of the broken surface of the composite showed greater interfacial adhesion between the glass fibers and polypropylene in the modified composite than that without modification. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1414–1420, 2005     

Thermal and mechanical properties of chitosan reinforced polyhydroxybutyrate composites

The article reports the results of studies on the effect of chitosan (0, 5, 10, 20, 30, and 40 wt %) on thermal and mechanical properties of poly(hydroxybutyrate) composites. The addition of chitosan causes an increase in the glass transition temperature (T_g) while a decrease in the enthalpy of fusion (ΔH_fus), crystallization (ΔH_cry) and percentage of crystallinity as determined by differential scanning calorimeter (DSC). The thermogravimetric analysis reveals that high amount of chitosan decreases the thermal stability of the composites. The Young's modulus of the composite increases and is high for the composite having 40 wt % of chitosan. Increase in the amount of chitosan decreases the elongation at break and impact strength of composites. Finally, the Young's modulus of the composites has been compared with the theoretical predictions. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Mechanical and thermal properties of SEBS‐g‐MA compatibilized halloysite nanotubes reinforced polyethylene terephthalate/polycarbonate/nanocomposites

In this study, the effect of maleic anhydride grafted styrene‐ethylene‐butylene‐styrene (SEBS‐g‐MA) content on mechanical, thermal, and morphological properties of polyethylene terephthalate/polycarbonate/halloysite nanotubes (PET/PC/HNTs) nanocomposites has been investigated. Nanocomposites of PET/PC (70 : 30) with 2 phr of HNTs were compounded using the counter rotating twin screw extruder. A series of formulations were prepared by adding 5–20 phr SEBS‐g‐MA to the composites. Incorporation of 5 phr SEBS‐g‐MA into the nanocomposites resulted in the highest tensile and flexural strength. Maximum improvement in the impact strength which is 245% was achieved at 10 phr SEBS‐g‐MA content. The elongation at break increased proportionately with the SEBS‐g‐MA content. However, the tensile and flexural moduli decreased with increasing SEBS‐g‐MA content. Scanning electron microscopy revealed a transition from a brittle fracture to ductile fracture morphology with increasing amount of SEBS‐g‐MA. Transmission electron microscopy showed that the addition of SEBS‐g‐MA into the nanocomposites promoted a better dispersion of HNTs in the matrix. A single glass transition temperature was observed from the differential scanning calorimetry test for compatibilized nanocomposites. Thermogravimetric analysis of PET/PC/HNTs nanocomposites showed high thermal stability at 15 phr SEBS‐g‐MA content. However, on further addition of SEBS‐g‐MA up to 20 phr, thermal stability of the nanocomposites decreased due to the excess amount of SEBS‐g‐MA. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42608.     

Dispersion and mechanical properties of a nanocomposite with an organoclay in an ionomer‐compatibilized LDPE matrix

Widely dispersed low density polyethylene (LDPE) based nanocomposites (Nc's) were obtained in the melt state thanks to their compatibilization with a zinc ionomer of poly(ethylene‐co‐methacrylic acid) (Pema‐Zn). The variables probed were the ionomer and organoclay content ranging from 0 to 20%, and from 0 to 10%, respectively. The TEM images showed that the organoclay is widely exfoliated. Furthermore, we report for the first time that the organoclay is concentrated in irregular zones. Taking into account the compatibility between MMT and the ionomer, it is plausible that the ionomer clusters are also concentrated in the organoclay‐rich regions. This heterogeneous microstructure has a positive effect on the mechanical properties since the Nc's are ductile, and the modulus increases were among the largest reported for LDPE, attaining a 160% increase with a 10% montmorillonite (MMT) content. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Morphology,thermal and mechanical performance of epoxy/polysulfone composites improved by curing with two different aromatic diamines

Epoxy/polysufone (PSF) composites cured with 4,4'-diaminodiphenyl sulfone (DDS) and 4,4'-diaminodiphenyl methane (DDM) were fabricated, and the effect of dual curing reaction of diamines with epoxy on morphology, mechanical, and thermal performance was investigated. DSC results indicated that DDM was more reactive than DDS and the activation energy decreased with the rising of DDM content. Structures with small domain size at the early stage of phase separation were fixed by the fast epoxy-DDM reaction. When the DDM content was elevated to a high level, large dual structures were changed to fine bicontinuous structures, which was favorable to improve the mechanical property. The mechanical performance of epoxy composites was enhanced and the maximum values were achieved when the DDM/DDS ratio was located at 75/25 (PSF/DDS0.25-DDM0.75). The flexural and tensile strength relative to epoxy/DDM system were enhanced more than those relative to epoxy/DDS, while the increase in toughness was the opposite. TGA measurement showed that thermal stability of epoxy/PSF composites was improved because of the restricting effect of continuous PSF domains on thermal motion of epoxy. DMA analysis exhibited two relaxation peaks for PSF/DDS0.25-DDM0.75, which could be attributed to the formation of phase separated morphology and epoxy network with different cross-link density.     

Accelerated weathering properties of compatibilized composites made from recycled HDPE and nonmetallic printed circuit board waste

The main aim of this work is to examine the influence of the contents of nonmetallic printed circuit board (PCB) waste component on the photodegradation of recycled high‐density polyethylene (rHDPE) composites. The properties tested were chemical changes, flexural properties, color stability, water absorption, leaching properties, and crystallinity changes of the composites after exposure to 2,000 h of accelerated weathering. Surface degradation for composites with nonmetallic PCB was less compared to unfilled rHDPE mainly because glass fibers covered almost the whole surface of specimens, acting as a protective layer, thus, slowing down the photodegradation reaction. Incorporation of compatibilizer in rHDPE/PCB composites had played an important role in resisting degradation due to UV exposure. All the composite samples became lighter in the early stages of weathering exposure; however, compatibilized composites showed less lightening and reduction on strength and modulus. Carbonyl index increases with exposure time indicating that the oxidation reaction continuously occurred during the aging process. Incorporation of compatibilizer had successfully reduced the water absorption uptake by the composites and effectively delayed some degradation properties of weathering. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43110.     

Effects of the moisture and fiber content on the mechanical properties of biodegradable polymer–sisal fiber biocomposites

The matrix of the composites that were used in this work was a commercial blend based on starch and cellulose derivatives. The biodegradable polymer was reinforced by short‐sisal fibers with a range in fiber content of 5–15 wt %. The effects of humidity on the diffusion coefficients, equilibrium moisture content, and mechanical properties were studied. Equations obtained from microscopic mass balances for diffusion in solids were used to predict the absorbed humidity in both components (the sisal fibers and biodegradable polymer) and in the composites as a function of time. Different model predictions of the composite diffusion coefficients as a function of the filler concentration were also examined, and they were found to be in agreement with the experimental results. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 4007–4016, 2004     

Artificial weathering effect on the structure and properties of polypropylene/polyamide‐6 blends compatibilized with PP‐g‐MA

The degradation of uncompatibilized and compatibilized PP/PA‐6 (70/30 wt %) with PP‐g‐MA under accelerated UV light was investigated using Fourier Transform Infrared Spectroscopy (FTIR) spectroscopy, melt flow index (MFI) tester, tensile test, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). FTIR analysis of the structure of the compatibilized and uncompatibilized blends after exposure to UV light showed the formation of photoproducts corresponding to both components. The MFI and mechanical results obtained revealed that photooxidation started primarily in PA‐6 rather than PP. In addition, the uncompatibilized blends exhibited a higher degradation rate compared to neat polymers for long exposure time, and the addition of PP‐g‐MA increased slightly their ageing rate in accordance with TGA data. Further, DSC analysis showed an increase in the crystallinity index and a decrease in the melting temperature of PP and PA‐6 after UV exposure either as neat polymers or as blend components. SEM micrographs of the cryo‐fractured surfaces of the samples illustrated the formation of cracks and fractures after UV irradiation. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41722.     

Thermal and mechanical characterization of linear low‐density polyethylene/wood flour composites

A linear low‐density polyethylene (LLDPE) matrix was modified with an organic peroxide and by a reaction with maleic anhydride (MAn) and was simultaneously compounded with untreated wood flour in a twin‐screw extruder. The thermal and mechanical properties of the modified LLDPE and the resulting composites were evaluated. The degree of crystallinity was reduced in the modified LLDPE, but it increased with the addition of wood flour for the formation of the composites. Significant improvements in the tensile strength, ductility, and creep resistance were obtained for the MAn‐modified composites. This enhancement in the mechanical behavior could be attributed to an improvement in the compatibility between the filler and the matrix. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2775–2784, 2003     

A compatibilized composite of recycled polypropylene filled with cellulosic fiber from recycled corrugated paper board: Mechanical properties,morphology, and thermal behavior

This article deals with the feasibility of using recycled corrugated paper board (rPF) as the reinforcing material for recycled plastics. The composites of recycled polypropylene (rPP) and rPF were prepared by extrusion compounding and injection molding, and the rPP/rPF composites compatibilized by maleic anhydride grafted PP (PP‐g‐MA), maleic anhydride grafted ethylene‐1‐octene copolymer (POE‐g‐MA), and maleic anhydride grafted styrene‐ethylene‐butylene‐styrene copolymer (SEBS‐g‐MA) were also prepared. The crystallization and melting behavior, mechanical properties, thermal stability, and morphology of these composites were studied. The results indicated that rPF promoted the crystallization, enhanced the strength and toughness of rPP/rPF composites to some extent while decreased thermal stability at the same time. PP‐g‐MA and POE‐g‐MA improved the dispersion and interface adhesion of rPF, and further upgraded the mechanical properties and vicat softening temperatures. Among these compatibilizers, PP‐g‐MA was most favorable to the strength improvement while POE‐g‐MA was most favorable to the toughness improvement. As for SEBS‐g‐MA, it had no obvious modification effect. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Effect of bamboo fibers with different coupling agents on the properties of poly(hydroxybutyrate-co-valerate) biocomposites

Green biocomposites were prepared via injection molding with poly(hydroxybutyrate-co-valerate) and natural bamboo fibers. Three types of coupling agents were used to modify the fibers, and the influence of different kinds of coupling agents was evaluated. The mechanical properties of the biocomposites varied with the type and content of the coupling agents. The water absorption and thermal properties of the composites were measured simultaneously after treatment with the coupling agents. Fourier transform infrared spectroscopy was employed to analyze the principle of fiber treatment with different coupling agents. The mechanical properties of the composites markedly improved, whereas the water absorption decreased after modification. Treatment with coupling agents only slightly influences the thermal properties but improved the crystallinity of the composites. Therefore, the interfacial compatibility between the fiber and matrix was enhanced after modification, with the silane coupling agent exhibiting the best effect. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47533.