Self-Reinforced Isotactic Polypropylene Prepared by Melt Vibration Injection Molding

Polypropylene (PP) has a good combination of properties, but at low temperatures it is friable and its impact ductility is very low. To improve impact strength, a vibration injection molding (VIM) technology was used to investigate the mechanical properties of polypropylene. Yield strength is upgraded with an increment in vibration frequency and a peak stands at a special frequency for VIM; the elongation at break and impact strength are also enhanced by increased vibration frequency. The wide-angle x-ray diffraction (WAXD) curves and the scanning electronic microscopy (SEM) micrographs have shown that, in the vibration field, the enhancement of mechanical properties is attributed to the occurrence of γ-phase crystals and more pronounced spherulite deformation than those seen in conventional injection moldings (CIM), and the smaller spherulites with the existence of β-phase crystals are favored for improving toughness. With the application of vibration injection molding, the mechanical properties of isotactic PP are improved. To prepare self-reinforcing and self-toughening polypropylene molded parts it has been concluded that high vibration frequency is required. Increasing vibration pressure amplitude obviously significantly improves the yield strength and impact strength.     

Influence of foaming technology on fibre breakage in long fibre-reinforced polypropylene composites parts

It is generally believed that the residual fibre length is one of the most important factors influencing on the mechanical properties of fibre-reinforced polymer matrix composites. In this study, long-glass fibre-reinforced polypropylene (LGFRPP) with initial fibre lengths of 12?mm was prepared and then moulded into parts via conventional injection moulding (CIM) and foamed injection moulding (FIM). The design of experiment (DOE) based on the Taguchi method was first used to determine the optimised processing conditions to increase the residual fibre length of the LGFRPP. The results indicated that foaming conditions have a substantial influence on the residual fibre length of the foamed samples. Based on the DOE, a set of optimised processing condition was selected, and two representative samples of CIM and FIM were carefully investigated using dynamical mechanical analysis, scanning electron microscopy, optical microscopy, etc. The experimental results further showed that the residual fibre length and the mechanical properties of the LGFRPP FIM components were better than those of the CIM components. It was also determined that there is a close relationship between the fibre breakage and the mechanical performance.     

Mechanical properties and morphology of polypropylene‐calcium carbonate nanocomposites prepared by dynamic packing injection molding

In this article, dynamic packing injection molding (DPIM) technology was used to prepare injection samples of Polypropylene‐Calcium Carbonate (PP/CaCO₃) nanocomposites. Through DPIM, the mechanical properties of PP/nano‐CaCO₃ samples were improved significantly. Compared with conventional injection molding (CIM), the enhancement of the tensile strength and impact strength of the samples molded by DPIM was 39 and 144%, respectively. In addition, the tensile strength and impact strength of the PP/nano‐CaCO₃ composites molded by DPIM increase by 21 and 514%, respectively compared with those of pure PP through CIM. According to the SEM, WAXD, DSC measurement, it could be found that a much better dispersion of nano‐CaCO₃ in samples was achieved by DPIM. Moreover, γcrystal is found in the shear layer of the DPIM samples. The crystallinity of PP matrix in DPIM sample increases by 22.76% compared with that of conventional sample. The improvement of mechanical properties of PP/nano‐CaCO₃ composites prepared by DPIM attributes to the even distribution of nano‐CaCO₃ particles and the morphology change of PP matrix under the influence of dynamic shear stress. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Hierarchic structure and mechanical property of glass fiber reinforced isotactic polypropylene composites molded by multiflow vibration injection molding

Maleic anhydride‐grafted polypropylene (Ma‐PP) and β nucleation agents (β‐NA) were used to modify the glass fiber (GF)/isotactic polypropylene (iPP) composite. The interface adhesion, degree of orientation, and crystalline morphologies of the PP/GF composites molded by multiflow vibrate‐injection molding (MFVIM) and conventional injection molding (CIM) were studied by polarized light microscopy (PLM), scanning electronic microscopy (SEM), and X‐ray measurements. Results prove that the interface adhesion was improved by the Ma‐PP; γ crystal was generated by the MFVIM due to the instant high pressure and shear during the multiflow; and a hierarchical structure which has a strengthened skin and a toughened core was formed. As a result, the final PP/GF/β‐NA composite has a 60% increase in tensile strength and 80% improvement in impact strength compare with the CIM pure PP/GF composite. Based on the observations, a modified model is proposed to interpret the strengthening and toughening mechanism. Our work paves the way to obtain high‐performance GF/iPP composites. POLYM. COMPOS., 38:2707–2717, 2017. © 2015 Society of Plastics Engineers     

Development of nanofibrous morphology in LDPE/LLDPE/PP blends and its effect on mechanical properties of blend films

Nanofibrous morphology has been observed in ternary blends of low density polyethylene (LDPE), linear low density polyethylene (LLDPE), and isotactic polypropylene (PP) when these were melt‐extruded via slit die followed by hot stretching. The morphology was dependent on the concentration of the component polymers in ternary blend LDPE/LLDPE/PP. The films were characterized by wide angle X‐ray diffraction (XRD), scanning electron microscopy (SEM), and testing of mechanical properties. The XRD patterns reveal that the β phase of PP is obtained in the as‐stretched nanofibrillar composites, whose concentration decreases with the increase of LLDPE concentration. The presence of PP nanofibrils shows significant nucleation ability for crystallization of LDPE/LLDPE blend. The SEM observations of etched samples show an isotropic blend of LDPE and LLDPE reinforced with more or less randomly distributed and well‐defined nanofibrils of PP, which were generated in situ. The tensile modulus and strength of LDPE/LLDPE/PP blends were significantly enhanced in the machine direction than in the transverse direction with increasing LLDPE concentration. The ultimate elongation increased with increasing LLDPE concentration, and there was a critical LLDPE concentration above which it increased considerably. There was a dramatic increase in the falling dart impact strength for films obtained by blow extrusion of these blends. These impressive mechanical properties of extruded samples can be explained on the basis of the formation of PP nanofibrils with high aspect ratio (at least 10), which imparted reinforcement to the LDPE/LLDPE blend. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effects of butyl acrylate modified polypropylene on structural and thermal properties of foamed polypropylene

In this work, the melt strength of PP matrix was reinforced by crosslinking‐modified PP (CM‐PP) which was yielded by peroxide‐initiated crosslinking of linear PP with butyl acrylate (BA). The nano‐silica aerogel (nano‐SiO₂) worked as a nucleating agent for foaming. The effects of CM‐PP with the various contents of BA on the foaming behavior and thermal property of PP were studied by measurements of density, thermal conductivity, Vicat softening temperature and SEM. The results showed that the foamed PP got the best properties when the crosslinking PP modified with the weight ratio of butyl acrylate was 10 wt %. The density of the obtained foamed PP with uniform closed cells was as low as 0.23 g/cm³, the thermal conductivity was 0.044 W/(m K), and the Vicat softening temperature was 120 °C. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44340.     

Effects of rosin‐type clarifying agent on the crystallization and compatibility of polypropylene and low density polyethylene

In this article, the influence of rosin‐type clarifying agent Nu‐(K + Na) and low density polyethylene (LDPE) on the crystallization process of polypropylene (PP) from the melt state was studied by differential scanning calorimeter and polarization microscope, and the effect of rosin‐type clarifying agent Nu‐(K + Na) on the compatibility of PP and LDPE was also investigated by dynamic mechanical analysis and scanning electron microscope. It was found that Nu‐(K + Na) decreased the fold surface energy and promoted the nucleation and crystallization of PP. With the cooperation of LDPE and Nu‐(K + Na) in PP, the chain fold free energy of PP was further decreased substantially, the crystallization rate of PP was increased more markedly, and the spherulites of PP became much smaller and dispersed more uniformly. At the same time, Nu‐(K + Na) improved the compatibility of PP and LDPE, and the LDPE was dispersed in PP more uniformly. Thus, the light scattering originating from the spherulites of PP and the LDPE disperse phase was reduced to great extent, and the transparency of PP was improved evidently. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 99: 1568–1575, 2006     

Structure and properties of polypropylene/low‐density polyethylene blends grafted with itaconic acid in the course of reactive extrusion

This study was concerned with the structural features and mechanical properties of polypropylene (PP)/low‐density polyethylene (LDPE) blends, which after compounding were modified by the free‐radical grafting of itaconic acid (IA) to produce [PP/LDPE]‐g‐IA in the course of reactive extrusion. To analyze the structural features of the [PP/LDPE]‐g‐IA systems, differential scanning calorimetry and relaxation spectrometry techniques were used. The data were indicative of the incompatibility of PP and LDPE in the [PP/LDPE]‐g‐IA systems on the level of crystalline phases; however, favorable interactions were observed within the amorphous phases of the polymers. Because of these interactions, the crystallization temperature of PP increased by 5–11°C, and that of LDPE increased by 1.3–2.7°C. The rapprochement of their glass‐transition temperatures was observed. The single β‐relaxation peak for the [PP/LDPE]‐g‐IA systems showed that compatibility on the level of structural units was responsible for β relaxation in the homopolymers used. Variations in the ratios of the polymers in the [PP/LDPE]‐g‐IA systems led to both nonadditive and complex changes in the viscoelastic properties as well as mechanical characteristics for the composites. Additions of up to 5 wt % PP strengthened the [PP/LDPE]‐g‐IA blended systems between the glass‐transition temperatures of LDPE and PP. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1746–1754, 2006     

One‐step green treatment of hemp fiber used in polypropylene composites

In this article, an eco‐friendly and cost effective surface treatment method is proposed for hemp fiber, enabling fabrication of hemp fiber/polypropylene (PP) composites, which show better mechanical properties than the PP composites containing untreated or alkali treated hemp fiber. Various techniques, such as scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), moisture analysis, and differential scanning calorimetry (DSC), are employed for the characterization of hemp fiber and polymer composites interface. Based on these results, the conventional alkali treatment of hemp fiber results in the damage of elementary fiber by eliminating parts of lignin and hemicellulose, which could be the reason for the decline of mechanical properties for the resulted polymer composites. On the contrary, water treatment cleans the fiber surface by effectively removing the water‐soluble polysaccharides while ensures minimum degradation on elementary fiber structure, which contributes to the improved mechanical properties of final polymer composites: the Young's modulus, fracture stress and fracture strain were enhanced by 3.66, 7.86, and 14.6%, respectively, when compared with untreated fiber reinforced composites. POLYM. COMPOS., 37:385–390, 2016. © 2014 Society of Plastics Engineers     

Recycling of poly(ethylene terephthalate) as polymer‐polymer composites

Microfibrillar reinforced composites (MFC) comprising an isotropic matrix from a lower melting polymer reinforced by microfibrils of a higher melting polymer were manufactured under industrially relevant conditions and processed via injection molding. Low density polyethylene (LDPE) (matrix) and recycled poly(ethylene terephthalate) (PET) (reinforcing material) from bottles were melt blended (in 30/70 and 50/50 PET/LDPE wt ratio) and extruded, followed by continuous drawing, pelletizing and injection molding of dogbone samples. Samples of each stage of MFC manufacturing and processing were characterized by means of scanning electron microscopy (SEM), wide‐angle X‐ray scattering (WAXS), dynamic mechanical thermal analysis (DMTA), and mechanical testing. SEM and WAXS showed that the extruded blend is isotropic but becomes highly oriented after drawing, being converted into a polymer‐polymer composite upon injection molding at temperatures below the melting temperature of PET. This MFC is characterized by an isotropic LDPE matrix reinforced by randomly distributed PET microfibrils, as concluded from the WAXS patterns and SEM observations. The MFC dogbone samples show impressive mechanical properties—the elastic modulus is about 10 times higher than that of LDPE and about three times higher than reinforced LDPE with glass spheres, approaching the modulus of LDPE reinforced with 30 wt% short‐glass fibers (GF). The tensile strength is at least two times higher than that of LDPE or of reinforced LDPE with glass spheres, approaching that of reinforced LDPE with 30 wt% GF. The impact strength of LDPE increases by 50% after reinforcement with PET. It is concluded that: (i) the MFC approach can be applied in industrially relevant conditions using various blend partners, and (ii) the MFC concept represents an attractive alternative for recycling of PET as well as other polymers.     

Effects of the chemical foaming agents,injection parameters,and melt‐flow index on the microstructure and mechanical properties of microcellular injection‐molded wood‐fiber/polypropylene composites

Wood‐fiber‐reinforced plastic profiles are growing rapidly in nonstructural wood‐replacement applications. Most manufacturers are evaluating new alternative foamed composites, which are lighter and more like wood. Foamed wood composites accept screws and nails better than their nonfoamed counterparts, and they have other advantages as well. For example, internal pressures created by foaming give better surface definition and sharper contours and corners than nonfoamed profiles have. In this study, the microfoaming of polypropylene (PP) containing hardwood fiber was performed with an injection‐molding process. The effects of different chemical foaming agents (endothermic, exothermic, and endothermic/exothermic), injection parameters (the mold temperature, front flow speed, and filling quantity), and different types of PP (different melt‐flow indices) on the density, microvoid content, physicomechanical properties, surface roughness, and microcell classification of microfoamed PP/wood‐fiber composites were studied. A maleic anhydride/polypropylene copolymer (MAH‐PP) compatibilizer was used with the intention of improving the mechanical properties of microfoamed composites. The microcell classification (from light microscopy) and scanning electron micrographs showed that an exothermic chemical foaming agent produced the best performance with respect to the cell size, diameter, and distance. The polymer melt‐flow index and the variation of the injection parameters affected the properties and microstructure of the microfoamed composites. The density of the microfoamed hardwood‐fiber/PP (with a high melt‐flow index) composites was reduced by approximately 30% and decreased to 0.718 g/cm³ with an exothermic chemical foaming agent. Tensile and flexural tests were performed on the foamed composites to determine the dependence of the mechanical properties on the density and microvoid content of the foamed specimens, and these properties were compared with those of nonfoamed composites. MAH‐PP improved the physicomechanical properties up to 80%. With an increase in the mold temperature (80–110°C), the surface roughness was reduced by nearly 70% for the foamed composites. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1090–1096, 2005     

Banded spherulites of HDPE molded by gas-assisted and conventional injection molding

Crystal morphologies of high density polyethylene (HDPE) with low molecular weight obtained by gas-assisted injection molding (GAIM), conventional injection molding (CIM), and spontaneous cooling, respectively, were studied by scanning electronic microscopy (SEM). It is found that banded spherulites are generated in the inner zone of GAIM parts and the outer zone of CIM parts but are absent in quiescent parts. According to the results, the representative morphologies of crystal change with gradual increment of instantaneous flow field in crystallization from non-banded spherulite to banded spherulite and then to oriented lamellae. This morphological evolution indicates that banded spherulites could be induced by flow field with certain intensity, which is confined by both an upper critical value and a lower one.     

玻璃纤维增强聚丙烯微孔注塑发泡成型

对不同填充形式下的3种聚丙烯(PP)进行Mucell微孔注射成型试验。根据扫描电镜(SEM)结果得出:3种PP发泡差别较大且出现了明显的分层现象。通过单因素四水平试验法,考察了在微孔注射成型过程中3种PP的熔体温度和注射速度对制品拉伸强度的影响。结果表明:随着熔体温度的增加,发泡材料的拉伸强度基本呈现上升趋势;较低的注射速度得到的样条残余玻纤长度较长,材料力学性能较好;进而得到了发泡样条的宏观力学性能与残余玻纤长度之间的关系。     

Strong and ductile poly(butylene adipate‐co‐terephthalate) biocomposites fabricated by oscillation shear injection molding

Poor interfacial properties and uncontrollable phase morphology encountered during the fabrication of poly(butylene adipate‐co‐terephthalate) (PBAT)/thermal plastic starch (TPS) biocomposites, result unfortunately in low mechanical performances and thus limit its applications. Here an approach in terms of phase morphology controlling, i.e., extrusion compounding followed by oscillation shear injection molding (OSIM), is proposed to construct in situ TPS fiber and skin‐core structure consisting of TPS fiber and droplet in skin layer, and spherical TPS in core layer, which tremendously benefits the mechanical properties. Specifically, the tensile strength, modulus and ductility for the biocomposites with various loadings of TPS, even when TPS loading as high as 55 wt %, outperform pure PBAT sample fabricated by conventional injection molding (CIM) with the increment of 51%, 308% in strength and modulus, respectively. Meanwhile, the elongation at breakage can maintain at 196%. The unprecedented establishment of high‐performance PBAT/TPS biocomposites is in great need for potential applications, such as green packaging. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43312.     

Mechanical properties and morphology of polyethylene–polypropylene blends with controlled thermal history

The effect of time–temperature treatment on the mechanical properties and morphology of polyethylene–polypropylene (PE–PP) blends was studied to establish a relationship among the thermal treatment, morphology, and mechanical properties. The experimental techniques used were polarized optical microscopy with hot‐stage, scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and tensile testing. A PP homopolymer was used to blend with various PEs, including high‐density polyethylene (HDPE), low‐density polyethylene (LDPE), linear low‐density polyethylene (LLDPE), and very low density polyethylene (VLDPE). All the blends were made at a ratio of PE:PP = 80:20. Thermal treatment was carried out at temperatures between the crystallization temperatures of PP and PEs to allow PP to crystallize first from the blends. A very diffuse PP spherulite morphology in the PE matrix was formed in partially miscible blends of LLDPE–PP even though PP was present at only 20% by mass. Droplet‐matrix structures were developed in other blends with PP as dispersed domains in a continuous PE matrix. The SEM images displayed a fibrillar structure of PP spherulite in the LLDPE–PP blends and large droplets of PP in the HDPE–PP blend. The DSC results showed that the crystallinity of PP was increased in thermally treated samples. This special time–temperature treatment improved tensile properties for all PE–PP blends by improving the adhesion between PP and PE and increasing the overall crystallinity. In particular, in the LLDPE–PP blends, tensile properties were improved enormously because of a greater increase in the interfacial adhesion induced by the diffuse spherulite and fibrillar structure. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 1151–1164, 2000     

Mechanical properties and morphology of crosslinked PP/PE blends and PP/PE/propylene–ethylene copolymer blends

Blending is an effective method for improving polymer properties. However, the problem of phase separation often occurs due to incompatibility of homopolymers, which deteriorates the physical properties of polyblends. In this study, isotactic polypropylene was blended with low-density polyethylene. Crosslinking agent and copolymers of propylene and ethylene (either random copolymer or block copolymer) were added to improve the interfacial adhesion of PP/LDPE blends. The tensile strength, heat deflection temperature, and impact strength of these modified PP/PE blends were investigated. The microstructures of polyblends have been studied to interpret the mechanical behavior through dynamic viscoelasticity, wide-angle X-ray diffraction, differential scanning calorimetry, picnometry, and scanning electron microscopy. The properties of crosslinked PP/PE blends were determined by the content of crosslinking agent and processing method. For the material blended by roll, a 2% concentration of peroxide corresponded to a maximum tensile strength and minimum impact strength. However, the mechanical strength of those products blended by extrusion monotonously decreased with increasing peroxide content because of serious degradation. The interfacial adhesion of PP/PE blends could be enhanced by adding random or block copolymer of propylene and ethylene, and the impact strength as well as ductility were greatly improved. Experimental data showed that the impact strength of PP/LDPE/random copolymer ternary blend could reach as high as 33.3 kg · cm/cm; however, its rigidity and tensile strength were inferior to those of PP/LDPE/block copolymer blend.     

The influence of the type of polypropylene and the length of the flow path on the structure and properties of injection molded parts with the weld lines

Weld lines, created in the areas of collision of two flow fronts of plastic in the injection mold cavity, are the reason of lower mechanical properties and a worse surface condition of molded parts. In the weld line area, the V‐shaped notch is formed and its shape and size depend on injection molding conditions and properties of processed polymer. Addition of the foaming agent to the polymer can be one of the way to improve conditions of melt streams welding due to the higher velocity of the colliding streams of unfilled polypropylene (PP) and PP filled with talc. The examinations of mechanical properties showed, however, lower tensile strength of porous parts compared to solid ones, but in the microscopic observation and measurements of the geometric structure of moldings, in the weld lines area, better surface conditions were achieved for samples made of the foamed polypropylene. The size of V‐notch, determined by the total height of the raw profile Pt, depends also on the length of polymer flow path from the gate to the weld line area. The values of Pt parameter increase with the length of the flow path, but this increase is smaller for foamed polypropylene. POLYM. ENG. SCI., 59:1710–1718 2019. © 2019 Society of Plastics Engineers     

Effect of grafting yield and molecular weight of m‐TMI‐grafted‐PP on the mechanical properties of wood fiber filled polypropylene composites

m‐Isopropenyl‐α, α‐dimethylbenzyl isocyanate (m‐TMI) was grafted on isotactic polypropylene (PP) using di‐cumyl peroxide as a reaction initiator under varying reaction conditions to yield m‐TMI‐g‐PP coupling agent with four sets of grafting yield and molecular weight. Grafting yield of the synthesized m‐TMI‐g‐PP were 1.80%, 2.01%, 9.05%, and 8.86% and molecular weight of the corresponding grafted polymer were 129,225; [Correction made here after initial online publication.] 187,240; 124,130; and 180,838, respectively. Rubberwood flour reinforced polypropylene composites were prepared using these coupling agents and tested for mechanical properties. m‐TMI‐g‐PP coupling agent with 9.09% grafting and 124230 M_w was found to give the highest tensile and flexural strengths. Flexural modulus of the coupled composites was higher than uncoupled composites. Interfacial region of the composites characterized by scanning electron microscope (SEM) suggest effective wetting of fiber by PP in the case of coupled composites. The effect of fiber loading on composites indicates continuous increment in tensile and flexural strengths in coupled composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44196.     

Influence of phase structure on impact toughening of isotactic polypropylene by metallocene‐catalyzed linear low‐density polyethylene

In the present study isotactic polypropylene (PP) and metallocene‐catalyzed linear low‐density polyethylene (mLLDPE) were blended together to obtain thermoplastic materials (compositions) with improved toughness. Structure–property relationships were determined for these compositions with the help of scanning electron microscopy (SEM). Special emphasis was made on tracing the morphological features that led to the optimum mechanical performance. A co‐continuous type of structure was found to have much superior toughness as compared to a dispersed‐matrix structural type, for blends comprised of the same components (PP and mLLDPE). The study showed the fascinating possibility of creating toughened PP blends by inducing a co‐continuous structure. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 1011–1018, 2000     

高强度低导热泡沫混凝土性能研究

在工程实践中,作为装配式建筑的墙体材料,既要有较好的保温隔热性能,又要满足一定的力学性能。轻质泡沫混凝土是一种很好的选择,但普通的泡沫混凝土材料在满足热工性能时其力学性能往往表现较差。本文提出一种高强度低导热泡沫混凝土制备方法,研究了水胶比、泡沫掺量、粉煤灰掺量和聚丙烯(PP)纤维掺量对泡沫混凝土的抗压强度和导热系数的影响,并采用扫描电镜(SEM)探究了粉煤灰和PP纤维对泡沫混凝土微观形貌的影响。结果表明:当水胶比为0.6、泡沫掺量为4%(质量分数,下同)、粉煤灰掺量为25%以及PP纤维掺量为0.2%时,泡沫混凝土的抗压强度较高且导热系数较低。