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1.
    
The effect of the delignification of hornbeam fibers on the mechanical properties of wood fiber–polypropylene (PP) composites was studied. Original fibers and delignified fibers at three levels of delignification were mixed with PP at a weight ratio of 40:60 in an internal mixer. Maleic anhydride (0.5 wt %) as the coupling agent and dicumyl peroxide (0.1 wt %) as the initiator were applied. The produced composites were then hot‐pressed, and specimens for physical and mechanical testing were prepared. The results of the properties of the composite materials indicate that delignified fibers showed better performance in the enhancement of tensile strength and tensile modulus, whereas the hardness of the composites was unaffected by delignification. Delignified fibers also exhibited better water absorption resistance. Notched impact strength was higher for delignified fiber composites, but it was reduced at higher delignification levels. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4759–4763, 2006  相似文献   

2.
    
Blends were prepared of poly(vinyl chloride) (PVC) with four different plasticizers; esters of aconitic, citric, and phthalic acids; and other ingredients used in commercial flexible PVC products. The thermal and mechanical properties of the fresh products and of the products after 6 months of aging were measured. Young's modulus of the PVC blends was reduced about 10‐fold by an increase in the plasticizer level from 15 to 30 phr from the semirigid to the flexible range according to the ASTM classification, but a 40‐phr level was required for PVC to retain its flexibility beyond 6 months. At the 40‐phr level, tributyl aconitate performed better than diisononyl phthalate (DINP) or tributyl citrate, in terms of lowering Young's modulus, both in the fresh materials and those aged for 6 months. The effects of the four plasticizers on the glass‐transition temperature (Tg) were similar, with Tg close to ambient temperature at the 30‐ and 40‐phr levels in freshly prepared samples and at 40–60°C in those aged for 6 months. The thermal stability of the PVC plasticized with DINP was superior among the group. Overall, tributyl aconitate appeared to be a good candidate for use in consumer products where the alleged toxicity of DINP may be an issue. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1366–1373, 2006  相似文献   

3.
    
A series of poly(vinyl chloride) (PVC)/green coconut fiber (GCF) composites, with dioctyl phthalate (DOP) or thermoplastic polyurethane (TPU) as a plasticizer, were prepared by melt mixing. Their properties were studied in the molten state with an advanced nonlinear harmonic testing technique; in the solid state, the hardness and impact resistance were evaluated, and scanning electron microscopy was used for fractured surfaces. The effect of the fiber loading was investigated, as well as the role of the plasticizer. PVC–GCF composites are heterogeneous materials that, in the molten state, exhibit essentially a nonlinear viscoelastic character, in contrast to pure PVC, which has a linear viscoelastic region up to 50–60% strain. The complex modulus increases with the GCF content but in such a manner that the observed reinforcement is at best of hydrodynamic origin, without any specific chemical (i.e., permanent) interaction occurring between the polymer matrix and the fibers. As expected, PVC offers good wetting of GCFs, as reflected by the easy mixing and the rheological and mechanical properties. Fibers can be incorporated into PVC up to a 30% concentration without any problem, with the PVC/plasticizer ratio kept constant. Higher GCF levels could therefore be considered. Replacing DOP in part with TPU gives some benefit in terms of impact resistance, likely because of the viscoelastic nature of the latter and the associated energy absorption effects. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007  相似文献   

4.
    
Ethanolamine and L ‐arginine treated wood flour were added to polyvinyl chloride (PVC) in order to improve the interphase between PVC and wood. The influence of the treatment on pH‐value changes and nitrogen fixation of the wood and mechanical properties of the composite were evaluated. The treatments changed the pH of wood from acidic to basic. The highest nitrogen fixation was measured for monoethanolamine and L ‐arginine treated wood flour at high concentrations. Tensile strength, elongation at break, and unnotched impact strength were improved by ethanolamine and L ‐arginine treatments considerably. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

5.
    
The use of rigid fillers to toughen polymers has received considerable attention in recent years. The role of the rigid particle here is that of debonding, at some stage, from the matrix, thus triggering dilatational processes similar to those observed in rubber‐toughened polymers. The role of particle size in these rigid filled composites has not been studied in great detail. In this work, volume strain measurements were carried out on a series of particulate composites based on polypropylene filled with calcium carbonate (CC) particles with average diameters of 0.07, 0.7, and 3.5 μm and filler volume fractions ranging from 0.05 to 0.30. The experimental results have shown a strong particle size effect. A model is proposed to take this effect into account, based upon the formation of an immobilized layer of polymer on the surface of the filler particles. The experimental results are consistent with a surface layer of 15–25 nm. The results are discussed in relation to the fracture behavior of these composites reported earlier. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 925–935, 2004  相似文献   

6.
    
The effect of oxidized polypropylene (OPP) as new compatibilizer on the water absorption and mechanical properties of wood flour–polypropylene (PP) composites were studied and compared with maleic anhydride grafted polypropylene (MAPP). The oxidation of PP was performed in the molten state in the presence of air. Wood flour, PP, and the compatibilizers (OPP and MAPP) were mixed in an internal mixer at temperature of 190°C. The amorphous composites removed from the mixer were then pressed into plates that had a nominal thickness of 2 mm and nominal dimensions of 15 × 15 cm2 with a laboratory hydraulic hot press at 190°C. Physical and mechanical tests showed that the wood flour–PP composites with OPP exhibited higher flexural and impact properties but lower water absorption than MAPP. All of the composites with 2% compatibilizers (OPP and MAPP) gave higher flexural and impact properties and lower water absorption compared to those with 4% compatibilizers. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

7.
    
A great amount of work has been done over the past few years to reuse the nonmetals recycled from waste printed circuit boards in polypropylene (PP) composites. This is because of the very fast generation rate of nonmetal pollution in the world each year and the very fast growing rate of PP applications in industries. This work focuses on the dynamic effects of nonmetals of different particle sizes on the tensile properties and reinforcing mechanisms of nonmetal/PP composites by in situ scanning electron microscopy tensile testing. The observed results show that the dominant deformation mechanism in pure PP is shear yielding. When fine nonmetals are filled into PP, mass microcracks are initiated. The glass fibers first resist the cracks and undertake the loading when they propagate. The crazes propagate slowly and then break the glass fibers. When coarse nonmetals are filled into PP, interfacial debonding and mass microcracks are initiated. A crack is either terminated when it meets another fiber–particulate bundle or branched into finer mass crazing. Interfacial debonding, crack initiation and propagation, and fiber pullout and breakage dissipate tremendous energy. These factors cause improvements in the strength and rigidity of nonmetal/PP composites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   

8.
Modified Mg(OH)2/polypropylene (PP) composites were prepared by the addition of functionalized polypropylene (FPP); and acrylic acid (AA) and by the formation of in situ FPP. The effects of the addition of FPP and AA and the formation of in situ FPP on the mechanical properties of Mg(OH)2/PP composites were investigated. Experimental results indicated that the addition of Mg(OH)2 markedly reduced the mechanical properties of PP. The extent of reduction in notch impact strength of PP was higher than that in flexural strength and tensile strength. However, tensile modulus and flexural modulus increased with increased Mg(OH)2 content. The addition of FPP facilitated the improvement in the flexural strength and tensile strength of Mg(OH)2/PP composites. The higher the Mg(OH)2 content was, the more significant the effect of FPP was. The incorporation of AA resulted in further increased mechanical properties, in particular the flexural strength, tensile strength, and notch impact strength of Mg(OH)2/PP composites containing high levels of Mg(OH)2. It not only improved mechanical properties but also increased the flame retardance of Mg(OH)2/PP composites. Although the mechanical properties of composites modified by the formation of in situ FPP were lower than those of composites modified by only the addition of AA in the absence of diamylperoxide, the mechanical properties did not decline with increased Mg(OH)2 content. Moreover, the mechanical properties increased with increasing AA content. The addition of an oxidation resistant did not influence the mechanical properties of the modified Mg(OH)2/PP composites. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2139–2147, 2003  相似文献   

9.
    
A novel grafted polymer was prepared in one step through free‐radical melt grafting in a single‐screw extruder. It was shown that the addition of styrene (St) to the melt‐grafting system as a comonomer could significantly enhance the grafting degree of methyl methacrylate (MMA) onto polypropylene (PP) and reduce the degradation of the PP matrix by means of Fourier transform infrared and melt flow rate testing, respectively. Then, the potential of using multimonomer‐grafted PP, which was designated PP‐g‐(St‐co‐MMA), as the compatibilizer in PP/poly(vinyl chloride) (PVC) blends was also examined. In comparison with PP/PVC blends, the average size of the dispersed phase was greatly reduced in grafted polypropylene (gPP)/PVC blends because of the addition of the PP‐g‐(St‐co‐MMA) graft copolymer. The tensile strength of the gPP/PVC blends increased significantly, and the impact strength was unchanged from that of the pure PP/PVC blends. The results of differential scanning calorimetry and scanning electron microscopy suggested that the compatibility of the PP/PVC blends was improved. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

10.
    
The Mg‐Al oxide precursor prepared by the calcination of Mg‐Al‐carbonated layered double hydroxide (LDH) at 500 K for 4 h is used as the host material, 2‐hydroxy‐4‐methoxybenzophenone‐5‐sulfonic acid (BP) is used as the guest material, BP‐intercalated LDH (LDH‐BP) is prepared by ion‐exchange method. The structure of LDH‐BP is characterized by X‐ray diffraction (XRD), Fourier transform infrared (FTIR), and thermogravimetry and differential thermal analysis (TG‐DTA). The thermal stability of PVC/BP, PVC/LDH, PVC/LDH‐BP composites, as well as pure PVC is investigated by conventional Congo Red test and dynamic thermal stability analysis in both the open and closed processing environments. According to XRD and FTIR, BP anions have been intercalated into interlayer galleries of LDH. TG‐DTA results show that the layer‐anionic interaction results in the improvement of the thermal stability of BP. Congo Red tests indicate that the addition of BP catalyzes the thermal degradation of PVC. A little amount of LDH (such as 1 phr) makes PVC more stable, but excessive addition accelerates the thermal degradation of PVC. The addition of LDH‐BP markedly improves the static thermal stability of PVC. The results of dynamic thermal stability tests in both the open and closed processing environments are consistent with that of Congo Red tests. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

11.
    
The influence of the crystalline areas observed in poly(vinyl chloride) (PVC) the mechanical and thermal properties of PVC plastisols was studied. Several industrial‐degree PVC resins were used to obtain a broad range of molecular weights and processing conditions for PVC plastisols. The gelation process was fully studied at different temperatures and was related to the existence of crystalline areas at high temperatures, even near the glass transition. A simple explanation of the phenomena observed during the gelation of plasticized PVC is proposed, according to the variation in the mechanical and thermal properties at different temperatures. The final gelation was obtained at 140–150°C, which was a lower temperature than those at the beginning of the thermal degradation process. The thermodynamic aspects of the gelation of plasticized PVC were mainly controlled by the PVC resin properties, whereas the plasticizer only influenced the diffusion and stability of the material. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 538–544, 2004  相似文献   

12.
    
This study was performed with commercially available phenyl trimethoxysilane (PTMS) and neoalkoxytitanate [i.e., neopentyl(diallyl)oxytri(dioctyl)phosphato titanate (LICA 12)] as coupling agents. PTMS and LICA 12 were used to treat talc and kaolin to compare their effects with untreated fillers upon incorporation into polypropylene (PP). Single‐filler PP composites (containing either talc or kaolin) and hybrid‐filler composites (containing a mix of both talc and kaolin) were compounded in a twin‐screw extruder and subsequently injection‐molded into dumbbells. The incorporation of PTMS and LICA 12 slightly decreased the tensile and flexural properties in terms of modulus and strength but increased the elongation at break for both single‐filler and hybrid‐filler composites. There was also a significant improvement in the impact strength of the composites, particularly those treated with LICA 12. The hybrid composites, through the synergistic coalescence of positive characteristics from talc and kaolin with the aid from chemical treatment provided an economically advantageous material with mechanical properties comparable to those of the single‐filler‐filled PP composites. Further investigations on flow and morphological properties were also done to correlate the mechanical properties of the single‐ and hybrid‐filler‐filled PP composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

13.
    
The physicomechanical properties, thermal properties, odor, and volatile organic compound (VOC) emissions of natural‐flour‐filled polypropylene (PP) composites were investigated as a function of the zeolite type and content. The surface area and pore structure of the natural and synthetic zeolites were determined by surface area analysis and scanning electron microscopy, respectively. With increasing natural and synthetic zeolite content, the tensile and flexural strengths of the hybrid composites were not significantly changed, whereas the water absorption was slightly increased. The thermal stability and degradation temperature of the hybrid composites were slightly increased with increasing natural and synthetic zeolite content. At natural and synthetic zeolite contents of 3%, the various odors and VOC emissions of the polypropylene/rice husk flour and polypropylene/wood flour hybrid composites were significantly reduced because of the absorption of the odor and VOC materials in the pore structures of the natural and synthetic zeolites. These results suggest that the addition of natural and synthetic zeolites to natural‐flour‐filled thermoplastic polymer composites is an effective method of reducing their odor and VOC emissions without any degradation of their mechanical and thermal properties. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008  相似文献   

14.
    
The effect of chopped rice husk (CRH) content on viscoelastic properties and crystallinity of polypropylene (PP) composites was investigated. Composites containing 0, 20, and 40 part per hundred plastics (php) of CRH into PP were prepared by twin‐screw extruder, with maleic anhydride‐grafted PP as the coupling agent. The viscoelastic behavior and the crystallinity of these composites have been studied by dynamic mechanical analysis as well as differential scanning calorimetry, respectively. By the incorporation of CRH into PP, the storage modulus (E′) was found to be increased progressively, whereas the mechanical loss factor (tan δ) decreased in a nonlinear manner. A self‐consistent analysis was proposed for the prediction of viscoelastic response of the interphase between PP matrix and CRH particles. A three‐phase model was applied in a reverse mode, and the viscoelastic behavior of the interphase was extracted and compared with the unfilled matrix. Differential scanning calorimetry results indicated that CRH influences crystallization temperature as well as the degree of crystallinity of the composites. An entrapped polymer within CRH filler and PP matrix was detected by scanning electron microscope, which can be attributed to the interfacial layer with a good adhesion between the main components. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

15.
    
Environmentally benign, low cost and abundantly available short pineapple leaf fibers (PALF), found mostly in the Tropical rain forest climates are ideal materials for manufacture of thermoplastic polymer‐matrix composites. Here, mechanical and thermal properties of composites of maleic anhydride grafted polypropylene (MA‐g‐PP) and chemically modified short PALF are studied as a function of different fiber lengths at 10 vol % fibers loading with fiber orientation in the longitudinal direction. The effects of fiber lengths and fiber loading on the morphological properties are assessed via observations by scanning electron microscopy. Fiber length of 6 mm oriented longitudinally at 10 vol % fibers loading in PP is the optimum and recommended composition, where 73% increase in impact properties, 37% increase in the flexural modulus, 33% increase in flexural strength, and 14% increase in vicat softening temperature are observed. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009  相似文献   

16.
    
The addition of organic fillers into thermoplastic polymers is an interesting issue, which has had growing consideration and experimentation during the last years. It can give rise to several advantages. First, the cost of these fillers is usually very low. Also, the organic fillers are biodegradable (thus contributing to an improved environmental impact), and finally, some mechanical and thermomechanical properties can be enhanced. In this study, the effect of the addition of different organic fillers on the mechanical properties and processability of an extrusion‐grade polypropylene were investigated. The organic fillers came from natural sources (wood, kenaf, and sago) and were compared to short glass fibers, a widely used inorganic filler. The organic fillers caused enhancements in the rigidity and thermomechanical resistance of the matrix in a way that was rather similar to the one observed for the inorganic filler. A reduction in impact strength was observed for both types of fillers. The use of an adhesion promoter could improve their behavior. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1906–1913, 2005  相似文献   

17.
    
Polypropylene (PP) composites filled with wood flour (WF) were prepared with a twin‐screw extruder and an injection‐molding machine. Three types of ecologically friendly flame retardants (FRs) based on ammonium polyphosphate were used to improve the FR properties of the composites. The flame retardancy of the PP/WF composites was characterized with thermogravimetric analysis (TGA), vertical burn testing (UL94‐V), and limiting oxygen index (LOI) measurements. The TGA data showed that all three types of FRs could enhance the thermal stability of the PP/WF/FR systems at high temperatures and effectively increase the char residue formation. The FRs could effectively reduce the flammability of the PP/WF/FR composites by achieving V‐0 UL94‐V classification. The increased LOI also showed that the flammability of the PP/WF/FR composites was reduced with the addition of FRs. The mechanical property study revealed that, with the incorporation of FRs, the tensile strength and flexural strength were decreased, but the tensile and flexural moduli were increased in all cases. The presence of maleic anhydride grafted polypropylene (MAPP) resulted in an improvement of the filler–matrix bonding between the WF/intumescent FR and PP, and this consequently enhanced the overall mechanical properties of the composites. Morphological studies carried out with scanning electron microscopy revealed clear evidence that the adhesion at the interfacial region was enhanced with the addition of MAPP to the PP/WF/FR composites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010  相似文献   

18.
    
In this study, the effect of the high‐energy mechanical milling of a mixture of poly(vinyl chloride) (PVC) with zinc borate (ZB) or ZB–aluminum trihydrate (ATH), a mixture of ZB and ATH, on the flame‐retardant and mechanical properties of ZB and ZB–ATH filled PVC was examined. The high‐energy mechanical milling of PVC/ZB and the PVC/ZB–ATH mixture produced chemical bonding between PVC and ZB or ZB–ATH, increasing the interfacial interaction of PVC/ZB and PVC/ZB–ATH blends, which resulted in a great increase in the limiting oxygen index, the impact and yield strengths, and the elongation at break of PVC/ZB and PVC/ZB–ATH blends. The results from ultraviolet spectroscopy and gas chromatography–mass spectroscopy show that mechanochemical modification of ZB and ZB–ATH much more effectively suppressed the release of aromatic compounds in PVC/ZB and PVC/ZB–ATH blends during burning. Mechanochemical modification provided an excellent route for the improvement of the flame‐retardant and mechanical properties of flame‐retardant‐additive‐filled PVC. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 753–762, 2003  相似文献   

19.
    
The morphology and mechanical properties of isotactic polypropylene (iPP) and poly(ethylene‐co‐methyl acrylate) (EMA) blends were investigated. Various EMA copolymers with different methyl acrylate (MA) comonomer content were used. iPP and EMA formed immiscible blends over the composition range studied. The crystallization and melting reflected that of the individual components and the crystallinity was not greatly affected. The size of the iPP crystals was larger in the blends than those of pure iPP, indicating that EMA may have reduced the nucleation density of the iPP; however, the growth rate of the iPP crystals was found to remain constant. The tensile elongation at break was greatly increased by the presence of EMA, although the modulus remained approximately constant until the EMA composition was greater than 20%. EMA with a 9.0% MA content provided the optimum effect on the mechanical properties of the blends. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 175–185, 2003  相似文献   

20.
    
Highly electrically conductive polypropylene (PP) composites were prepared by melt mixing using tin–lead (Sn‐Pb) alloy as conducting fillers. Two Sn‐Pb alloys, Sn‐Pb (20/80) and Sn‐Pb (40/60), were used for comparison. The effects of Sn‐Pb loading and molding temperature on electrical conductivity and mechanical properties of composites were investigated. It was found that both factors had significant effect on electrical conductivity of the final Sn‐Pb/PP composite. It was interesting to observe that the molding temperature could control the formation of long‐range conducting paths. The mechanism has been explored through the nonequilibrium phase behavior of Sn‐Pb alloy. The influence of Sn‐Pb loading on mechanical properties of Sn‐Pb/PP composites was also investigated. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011  相似文献   

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