Studies on morphology and mechanical properties of PP/HIPS blends from postconsumer plastic waste

The aim of this work was to study the compatibilizing effect of the triblock copolymer poly(styrene‐b‐ethylene‐co‐butylene‐b‐styrene) (SEBS) on the morphology and mechanical properties of virgin and recycled polypropylene/high‐impact polystyrene (PP/HIPS) blends. The components of the blend were obtained from municipal plastics waste (MPW), with the PP obtained from blue mineral water bottles, symbolized as PP_b, and the HIPS from disposable cups. These materials were preground, washed only with water, dried with hot air, and ground again (PP_b) or agglutinated (HIPS). Blends of PP_b and HIPS in three weight ratios (6:1, 6:2, and 6:3) were prepared, and three concentrations of SEBS (5.0, 6.0, and 6.7% w/w) were used for investigations of its compatibilizing effect. Scanning electron microscopy (SEM) showed that SEBS reduced the diameter of HIPS dispersed particles that were globular and fibril shaped, along with improving the adhesion between the dispersed phase and the matrix. On the other hand, SEBS interactions with PP_b and HIPS influenced the mechanical properties of the compatibilized PP_b/HIPS/SEBS blends. The optimal concentration of SEBS was 5 wt % for application to composite films with similar characteristics to synthetic paper. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 747–751, 2003     

Mechanical properties of biorenewable fiber/plastic composites

Plastic fiber composites, consisting of polypropylene (PP) or polyethylene (PE), and pinewood, big blue stem (BBS), soybean hulls, or distillers dried grain and solubles (DDGS), were prepared by extrusion. Young's modulus, tensile and flexural strengths, melt flow, shrinkage, and impact energy, with respect to the type, amount, and size of fiber on composites, were evaluated. Young's moduli under tensile load of wood, BBS, and soybean‐hull fiber composites, compared with those of pure plastic controls, were either comparable or higher. Tensile strength significantly decreased for all the PP/fiber composites when compared with that of the control. Strength of BBS fiber composites was higher than or comparable to that of wood. When natural fibers were added there was a significant decrease in the melt flow index for both plastic/fiber composites. There was no significant difference in the shrinkage of all fiber/plastic composites compared to that of controls. BBS/PE plastic composites resulted in higher notched impact strength than that of wood or soybean‐hull fiber composites. There was significant reduction in the unnotched impact strength compared to that of controls. BBS has the potential to be used as reinforcing materials for low‐cost composites. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 2484–2493, 2004     

The role of additives in the manufacture of sheets of unsaturated polyester and postconsumer unsaturated polyester/glass fiber composites: Mechanical and dynamic mechanical properties

The storage of postconsumer glass fiber reinforced unsaturated polyester composite impacts negatively on the environment because of the long lifetime and the volume/amount ratio of residuals, which are important aspects to be considered. Two types of additives were employed as an attempt to improve the mechanical properties of sheets manufactured with ground postconsumer glass fiber reinforced orthophthalic unsaturated polyester resin composite and virgin orthophthalic unsaturated polyester resin, a silane‐coupling agent and an organic dispersant. Flexural and impact tests, and dynamic mechanical analyses, demonstrated that the coupling agent increased the mechanical properties, while the dispersant decreased these properties, compared to material without either additive. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 1834–1839, 2004     

Correlation of viscosity ratio,morphology, and mechanical properties of polyamide 12/natural rubber blends via reactive compatibilization

Natural rubber (NR)-modified polyamide 12 (Nylon12/NR) was produced by melt blending Nylon12 and NR in the presence of polystyrene/maleated natural rubber (PS/MNR) copolymer as a reactive compatibilizer. The influence of compatibilizer loading on viscosity ratio, morphology, and mechanical properties of the blends was investigated. As a consequence of the reactive blend between Nylon12 and maleated NR in PS/MNR, the formation of amide and succinimide linkages was set at rubber-Nylon12 interfaces. Thus the dispersion of rubber particles was improved, and the particle coalescence was prevented so that the fine morphology with good interfacial adhesion was stabilized. This also resulted to enhance the blend viscosity and to lower viscosity ratio. The data revealed strong correlation between low viscosity ratio and fine spherical morphology of the compatibilized blends. An optimum PS/MNR compatibilizer content was at 7 phr to produce good dispersion of small rubber domains (size ≤0.3 μm) in Nylon12 matrix. Thermal properties by DSC revealed that crystallization temperature of Nylon12 was lowered by the presence of NR and crystallinity of Nylon12 was slightly affected by the PS/MNR content. An enhancement of mechanical properties, especially the impact energy was observed without suffering the tensile and flexural properties. Compared to the neat Nylon12, the compatibilized blends showed an increase in impact energy by a factor of 5. This large enhancement is successfully interpreted in term of the toughening effect by rubber phase of suitable dispersed size and the interparticle distance.     

Morphology and mechanical properties of polypropylene/high‐impact polystyrene blends from postconsumer plastic waste

The compatibilizing effect of the triblock copolymer poly(styrene‐b‐ethylene‐co‐butylene‐b‐styrene) (SEBS) on the morphological and mechanical properties of virgin and recycled polypropylene (PP)/high‐impact polystyrene (HIPS) blends was studied, with the properties optimized for rigid composite films. The components of the blend were obtained from municipal plastic waste, PP being acquired from mineral water bottles (PP_b) and HIPS from disposable cups. These materials were preground, washed only with water, dried with hot air, and ground again (PP_b) or agglutinated (HIPS). Blends with three different weight ratios of PP_b and HIPS (6:1, 6:2, and 6:3) were prepared, and three different concentrations of SEBS (5, 6, and 7 wt %) were used for investigations of its compatibilizing effect. Scanning electron microscopy showed that SEBS reduced the diameter of dispersed HIPS particles in the globular and fibril shapes and improved the adhesion between the disperse phase and the matrix. However, SEBS interactions with PP_b and HIPS influenced the mechanical properties of the compatibilized PP_b/HIPS/SEBS blends. An adequate composition of PP/HIPS, for both virgin and recycled blends, for applications in composite films with characteristics similar to those of synthetic paper was obtained with a minimal amount of SEBS and a maximal HIPS/PP ratio in the range of concentrations studied. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2861–2867, 2003     

Effect of chemical reagents on the mechanical properties of natural fiber polypropylene composites

Chemical resistance of natural fiber (wood flour, rice hulls, kenaf fiber, and newsprint) polypropylene composites was studied in terms of their weight loss and reduction of mechanical properties after 7 days immersion in chemical reagents. Composites containing 25 and 50% of various natural fibers and polypropylene were prepared and immersed in NaOH (10%), NaClO (bleach solution) (13%), HCl (10%), H₂O₂ (3%), soap solution (1%), and acetone. Results indicated that H₂O₂, soap solution, and acetone had very negligible effects on all composites. On the other hand, the effects of NaClO and HCl were found to be statistically significant. Different fibers exhibited different behaviors regarding their chemical resistance. Rice hulls composites were considerably affected by NaOH, whereas the same chemical reagent was ineffective on other fibers. The effects of bleach solution and HCl on the mechanical performance of the composites were found to be critical. Generally, it was concluded that bleach and acids had the highest effects on natural fiber polypropylene composites. POLYM. COMPOS. 27:563–569, 2006. © 2006 Society of Plastics Engineers     

Effect of extruder elements on fiber dimensions and mechanical properties of bast natural fiber polypropylene composites

Illusions and facts about aspect ratio and the corresponding mechanical properties of the polypropylene flax are studied in this work. Selection of extruder elements controls significantly the fiber final dimensions. Hence, the load transfer efficiency can be improved. Different extruder layouts are tried. First and second trials investigate the mixing degree effect using kneading elements with eight and four kneading elements, respectively. The third and fourth trials keep four kneading blocks but differentiate in using multiprocessing element MPE and toothed elements, respectively. All the four configurations are tested at different shearing rates namely 100, 200, and 300 rpm and different fiber loadings 10, 20, and 30 wt %. Polypropylene (PP) with high flowing properties and slivers flax natural fibers are used. The output extruded strands are mechanically tested. The third and fourth configurations showed superiority to the normal kneading profiles regarding the mechanical properties. Samples of composites are withdrawn after each processing extruder element to study the effect of this element on the fiber dimension. Measurement of extracted fibers is carried out by two methods namely dynamic image analysis machine and secondly normal microscopic investigation. Weibull distributions are defined for fiber geometry distributions for the different locations on the extruder configuration. Also, the effect of the shear rate and the extruder configuration on the final dimensions of the fibers extracted from the composite. The results show the correlation between extruder configuration and fiber aspect ratio and hence the composite overall strength. However, further processing like injection molding erases the pre‐extrusion effect. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40435.     

Effect of natural fibers on thermal and mechanical properties of natural fiber polypropylene composites studied by dynamic mechanical analysis

The present study deals with the effects of natural fibers on thermal and mechanical properties of natural fiber polypropylene composites using dynamic mechanical analysis. Composites of polypropylene and various natural fibers including kenaf fibers, wood flour, rice hulls, and newsprint fibers were prepared at 25 and 50% (by weight) fiber content levels. One and two percent maleic anhydride grafted polypropylene was also used as the compatibilizer for composites containing 25 and 50% fibers, respectively. Specimens for dynamic mechanical analysis tests were cut out of injection‐molded samples and were tested over a temperature range of ?60 to +120°C. Frequency of the oscillations was fixed at 1 Hz and the strain amplitude was 0.1%, which was well within the linear viscoelastic region. The heating rate was 2°C/min for all temperature scan tests. Storage modulus (E′), loss modulus (E″), and mechanical loss factor (tan δ) were collected during the test and were plotted versus temperature. An increase in storage and loss moduli and a decrease in the mechanical loss factor were observed for all composites indicating more elastic behavior of the composites as compared with the pure PP. Changes in phase transition temperatures were monitored and possible causes were discussed. Results indicated that glass transition was slightly shifted to lower temperatures in composites. α transition temperature was higher in the case of composites and its intensity was higher as well. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 4341–4349, 2006     

Thermal and mechanical properties of wood flour–polystyrene blends from postconsumer plastic waste

Polystyrene (PS) from packing materials and plastic cups was reinforced with 30 and 50% wood flour through a blending process with and without a commercial compatibilizing agent. The processability of the pure recycled polystyrene (rPS) and wood–rPS composites was studied in terms of the torque of the mixing process; this was then compared with that of a commercial virgin multipurpose PS. The physical and mechanical properties were compared with those of the virgin PS reinforced with 30 and 50% wood flour. The results show that the mechanical properties of the pure and reinforced rPS did not decrease with respect to the virgin PS, and in terms of the impact strength, the rPS was superior to the virgin plastic. The mechanical properties were not affected by the commercial compatibilizing agent, but the torque of the blends was significantly lower with the compatibilizer. Differential scanning calorimetry (DSC) and dynamic mechanical analysis were used to study the glass‐transition temperature (T_g) of both the pure virgin PS and pure rPS and the wood flour–PS composites. The T_g values of the rPS and wood–rPS composites were higher than those of the virgin PS and wood–virgin PS composites. The use of rPS increased the stiffness and flexural modulus of the composites. Thermogravimetric analysis revealed that the thermal stability of rPS and its composites was slightly greater than that of the virgin PS and its composites. These results suggest that postconsumer PS can be used to obtain composite materials with good mechanical and thermal properties. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Mechanical properties of sisal natural fiber composites according to strain rate and absorption ratio

The effects of strain rate and water absorption properties can be used to evaluate the environmental degradation of sisal fiber reinforced polymer–matrix composites. Composites of vinylester and epoxy resin, reinforced by sisal fiber, were manufactured using the RTM method. To examine how the mechanical properties change with different surface treatments of a fiber, three fibrous composites with nontreated, permanganate, and silane treatments were compared in this experiment. Material fracture occurred as the brittleness hardened due to an increase in strain rate. The tensile strength was the largest in the permanganate‐treated epoxy composites, while the untreated vinylester had high elongation and fracture energy. The highest tensile strength value occurred at a 30% absorption ratio. POLYM. COMPOS., © 2011 Society of Plastics Engineers.     

Improving the foaming and mechanical properties of the in situ microfiber-reinforced polyethylene terephthalate/polypropylene composites through compatibilization

The in situ microfiber-reinforced polyethylene terephthalate/isotactic polypropylene (15/85, w/w) composite (PET/iPP MRC) was successfully obtained through the micro-nano-laminating co-extrusion by using polypropylene-grafted-glycidyl methacrylate (PP-g-GMA) as a compatibilizer. The effect of the compatibilizer on the rheological behavior, micromorphology of PET/iPP MRC, foaming capability and the mechanical properties of foamed PET/iPP MRC was investigated. Extensional rheology measurement revealed the strain hardening of PET/iPP MRC is more obviously than iPP and with compatibilizer added. Scanning electron microscope observation indicated that the introduction of PP-g-GMA compatibilizer can improve the compatibility between PET and PP and subsequently lead to the decrease of diameter of PET microfibers. In addition, the incorporating of PP-g-GMA compatibilizer can also decrease the diameter and enhance the cell density of PET/iPP MRC cell. Both the tensile strength and the impact strength of the PET/iPP MRC foam are higher than that of the iPP foam, and improved with the compatibilizer added.     

Sustainable conducting polymer composites: study of mechanical and tribological properties of natural fiber reinforced PVA composites with carbon nanofillers

ABSTRACT

Ball milled jute fiber (JF) was added to Polyvinyl Alcohol (PVA)/20 wt.% multi-layer graphene (MLG) composites in various proportions (0, 5, 10, 15 and 20 wt.%) to prepare sustainable and biodegradable conducting polymer composites. Also, PVA/17.5wt.%MLG/2.5wt.%MWCNT/20wt.% JF composite was prepared for comparison purpose. A dynamic mechanical analysis of the composites was conducted to analyze their viscoelastic nature. The electrical conductivity of the composites was measured to study their suitability for various applications. Jute reinforcement increased the electrical conductivity of PVA/MLG nanocomposites. The PVA/20wt.%JF/17.5wt.%MLG/2.5wt.%MWCNT hybrid composite had the highest electrical conductivity of 3.64 × 10^?4 S/cm among all the composites prepared. Multilayered structures of the hybrid composite films were made by hot-pressing, and their effectiveness in electromagnetic interference shielding was tested. The shielding effectiveness of the composites decreased with jute addition. The wear resistance of PVA/MLG/JF composites increased with an increase in the jute content up to an optimum value of 10 wt.%, and then it started deteriorating.     

Deformation mechanisms and mechanical properties of modified polypropylene/wood fiber composites

Mechanical properties and deformation mechanisms of polypropylene (PP)/wood fiber (WFb) composites modified with maleated polypropylene as compatibilizer and styrene-butadiene rubber (SBR) as impact modifier have been studied. The addition of maleated polypropylene to the unmodified polypropylene/wood fiber composite enhances the tensile modulus and yield stress as well as the Charpy impact strength. SBR does not cause a drop in the tensile modulus and yield strength because of the interplay between decreasing stiffness and strength by rubber modification and increasing stiffness and strength by good interfacial adhesion between the matrix and fibers. The addition of both maleated polypropylene and rubber to the polypropylene/wood fiber composite does not result in an improvement of effects based on maleated polypropylene and rubber, which includes possible synergism. The deformation mechanisms in unmodified polypropylene/wood fiber composite are matrix brittle fracture, fiber debonding and pullout. A polymeric layer around the fibers created from maleated polypropylene may undergo debonding, initiating local plasticity. Rubber particle cavitation, fiber pullout and debonding were the basic failure mechanisms of rubber-toughened polypropylene/wood fiber composite. When maleated polypropylene was added to this composite, fiber breakage and matrix plastic deformation took place. Polym. Compos. 25:521–526, 2004. © 2004 Society of Plastics Engineers.     

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

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

Effect of hybridization and compatibilization on the mechanical properties of recycled polypropylene‐hemp composites

Hemp fibers and particles, with different sizes and contents, were used to make hybrid composites based on recycled polypropylene (PP). In particular, the effect of maleated polypropylene (MAPP) addition on the morphology and mechanical properties is reported. The results show that better adhesion is obtained with MAPP addition. In general, fiber content and size had a substantial effect on the tensile, flexural, torsion, and impact properties of the resulting composites. Although, adding MAPP to the samples improved the impact strength of the composites, the values were always lower than neat PP. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Interphase effects on the mechanical and physical aspects of natural fiber composites

The interaction and adhesion between the fiber and matrix has a significant effect in determining the mechanical and physical behavior of fiber composites. The effect of the interface and interphase depends on several factors such as chemical composition (functional groups), molecular structure characteristics (branching, molecular weight distribution, cross-linking), and details of its physical state (above or below T_g, nature and degree of crystallinity). Natural fibers have complex and varying chemical structures that have uneven surface topographies. This creates difficulties in using single fiber composite testing to accurately evaluate the interfacial shear strengths, except for comparisons. A review of our interphase related research in natural fiber composites is presented. When using coupling agents it is well known that the tensile and flexural strengths increase dramatically in natural fiber reinforced composites. However, in the case of modulus, the results are more complex. For two ethylene-propylene impact copolymers, the uncoupled systems had much higher Young's moduli than the coupled systems. The dynamic storage moduli of the uncoupled impact polymers were higher than the coupled composites at temperatures up to about 50°C. At higher temperatures the presence of the coupling agent resulted in higher storage moduli. Transcrystallinity may play an important role in this phenomenon. Creep and other long-term properties are also affected by the quality of the interphase, although the level of improvement decreases with an increase in the molecular weight of the matrix polymer. Coupling agents reduced the rate of water absorption and the moduli were less affected in blends with a higher concentration of coupling agents.     

反应性增容对PP/纳米SiO2性能的影响

研究了反应性增容对聚丙烯(PP)／纳米SiO2复合材料结晶和流变性能的影响。反应性增容使PP的结晶峰温明显提高,结晶速率增大,球晶细化;复合材料的储能模量、损耗模量和复数黏度明显增大,熔体流动速率减小。在环氧功能化纳米SiO2质量分数为3％,反应性增容剂氨基化PP质量分数为10％时,复合材料的结晶峰温从115.8℃升到125．6℃,熔体流动速率从11．0g/10 min降到8．5 g/10 min。     

Fundamental studies on wood–plastic composites: Effects of fiber concentration and mixing temperature on the mechanical properties of poplar/PP composite

Wood fibers are increasingly being used as reinforcement in commercial thermoplastic composites due to their low cost, high specific properties and renewable nature. The ultimate goal of our research was to find a fundamental understanding of the mechanical behavior of poplar/polypropylene (PP) composites. The effect of wood fiber concentrations and mixing temperature on the mechanical properties of composites, prepared by using MAPP as the coupling agent, was investigated. In the sample preparation, four levels of fiber loading (10, 20, 30, and 40 wt%) and three compounding temperatures (180, 190, and 200^oC) were used. Most major changes in composite performance occurred at fiber contents above 30%. The results clearly showed that the fiber loading of 30 and 40 wt% at 190^oC was provided adequate reinforcement to increase the tensile and flexural strength of the PP powder. The modulus also increased with increasing the fiber content, because poplar fibers are believed to be more rigid than polymer. However the addition of wood fibers resulted in a decrease in elongation and impact properties of the composites. The FTIR spectroscopy showed that the copolymer was bonded to the fibers by ester linkages and hydrogen bonds at 1705–1735 cm⁻¹. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Effect of fiber pretreatment condition on the interfacial strength and mechanical properties of wood fiber/PP composites

The effect of fiber surface pretreatment on the interfacial strength and mechanical properties of wood fiber/polypropylene (WF/PP) composites are investigated. The results demonstrate that fiber surface conditions significantly influence the fiber–matrix interfacial bond, which, in turn, determines the mechanical properties of the composites. The WF/PP composite containing fibers pretreated with an acid–silane aqueous solution exhibits the highest tensile properties among the materials studied. This observation is a direct result of the strong interfacial bond caused by the acid/water condition used in the fiber pretreatment. Evidence from coupling chemistry, rheological and electron microscopic studies support the above conclusion. When SEBS‐g‐MA copolymer is used, a synergistic toughening effect between the wood fiber and the copolymer is observed. The V‐notch Charpy impact strength of the WF/PP/SEBS‐g‐MA composite is substantially higher than that of the WF/PP composite. The synergistic toughening mechanisms are discussed with respect to the interfacial bond strength, fiber‐matrix debonding, and matrix plastic deformation. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 1000–1010, 2000