Self‐reinforcement of high‐density polyethylene/low‐density polyethylene prepared by oscillating packing injection molding under low pressure

This article reports the toughness improvement of high‐density polyethylene (HDPE) by low‐density polyethylene (LDPE) in oscillating packing injection molding, whereas tensile strength and modulus are greatly enhanced by oscillating packing at the same time. Compared with self‐reinforced pure HDPE, the tensile strength of HDPE/LDPE (80/20 wt %) keeps at the same level, and toughness increases. Multilayer structure on the fracture surface of self‐reinforced HDPE/LDPE specimens can be observed by scanning electron microscope. The central layer of the fracture surface breaks in a ductile manner, whereas the break of shear layer is somewhat brittle. The strength and modulus increase is due to the high orientation of macromolecules along the flow direction, refined crystallization, and shish‐kebab crystals. Differential scanning calorimetry and wide‐angle X‐ray diffraction find cocrystallization occurs between HDPE and LDPE. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 799–804, 1999     

Bi‐axial self‐reinforcement of high‐density polyethylene induced by high‐molecular weight polyethylene through dynamic packing injection molding

Previously, bi‐axial self‐reinforcement of high‐density polyethylene (HDPE) was achieved through a uni‐axial shear stress field introduced by dynamic packing injection molding technology. Here, further improvement of tensile strength along the flow direction (MD) was achieved by blending a small amount of high‐molecular‐weight polyethylene (HMWPE) with HDPE, while the tensile strength along the transverse direction (TD) still substantially exceeded that of conventional moldings. Tensile strengths in both flow and transverse directions were considerably enhanced, with improvements from 23 MPa to 76 MPa in MD and from 23 MPa to 31 MPa in TD. The effect of HMWPE content and molding parameters on tensile properties was also investigated. The tensile strength along MD was highly dependent on HMWPE content, oscillating cycle, mold temperature, melt temperature and packing pressure, while that along TD was insensitive to composition and processing parameters within the selected design space. According to the stress–strain curves, samples with HMWPE produced by dynamic packing injection molding had a special tensile failure mode in MD, different from both typical plastic and brittle failure modes. There were no yielding and necking phenomena, which are characteristic during tensile testing of plastic materials, but there was still a considerably higher elongation compared to those of brittle materials. However, in TD, all dynamic injection molding samples exhibited plastic failure as did typical conventional injection molding samples. Copyright © 2006 Society of Chemical Industry     

Biaxially self‐reinforced high‐density polyethylene prepared by dynamic packing injection molding. I. Processing parameters and mechanical properties

Uniaxial oscillating stress field by dynamic packing injection molding (DPIM) is well established as a means of producing uniaxially self‐reinforced polyethylene and polypropylene. Here, the effects on the mechanical properties of high‐density polyethylene (HDPE) in both flow direction (MD) and transverse direction (TD) of packing modules and processing parameters in DPIM are described. Both biaxially and uniaxially self‐reinforced HDPE samples are obtained by uniaxial shear injection molding. The most remarkable biaxially self‐reinforced HDPE specimens show a 42% increase of the tensile strength in both MD and TD. The difference of stress–strain behavior and impact strength between MD and TD for the DPIM moldings indicates the asymmetry of microstructure in the two directions. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1584–1590, 2004     

Biaxially self‐reinforced high‐density polyethylene prepared by dynamic packing injection molding. II. Microstructure investigation

Differential scanning calorimetry, wide‐angle X‐ray diffraction, small‐angle X‐ray scattering, and transmission electron microscope are employed to study the microstructure of biaxially self‐reinforced high‐density polyethylene (HDPE) prepared in uniaxial oscillating stress field by dynamic packing injection molding. The results indicate that the biaxial self‐reinforcement of HDPE is mainly due to the existence of interlocking shish‐kebab morphology (i.e., zip fastener structure), along with the orientation of lamellae and molecular chains and the enhanced crystallinity. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1591–1596, 2004     

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     

Biaxial self‐reinforcement of isotactic polypropylene prepared in uniaxial oscillating stress field by injection molding. I. Processing conditions and mechanical properties

This research explores the longitudinal and latitudinal mechanical properties of injection‐molded isotactic polypropylene (iPP) prepared in a uniaxial oscillating stress field by oscillating packing injection molding (OPIM). The methods, processing conditions, and mechanical test results for iPP by conventional injection molding (CIM) and OPIM are described. The mechanical properties in the flow direction (MD) and transverse direction (TD) of the OPIM moldings indicate three types of self‐reinforced iPP moldings. The pronounced biaxially self‐reinforced iPP specimens exhibit a 55–70% increase of the tensile strength and more than a fourfold increase of the impact strength in the MD, together with more than a 40% increase of the tensile strength and a 30–40% increase of the impact strength in the TD. The OPIM moldings show different stress–strain behavior in the MD and TD. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 1906–1910, 2000     

Crystallization behavior and molecular orientation of high density polyethylene parts prepared by gas‐assisted injection molding

The dependence of hierarchy in crystalline structures and molecular orientations of high density polyethylene parts with different molecular weights molded by gas‐assisted injection molding (GAIM) was intensively examined by scanning electron microscopy, two‐dimensional wide‐angle X‐ray scattering as well as dynamic rheological measurements. The non‐isothermal crystallization kinetics of the samples were also analyzed with a differential scanning calorimeter at various scanning rates. It was found that oriented lamellar structure, shish‐kebab and common spherulites were formed in different regions of the GAIM samples. The scanning electron microscope observations were consistent with the two‐dimensional wide‐angle X‐ray scattering results and showed that the molecular chains near the mold wall had strong orientation behavior, revealing the distribution of the shear rate of the GAIM process. The differences in crystal morphologies can be attributed to molecular weight differences as well as their responses to the external fields during the GAIM process. The formation mechanism of the shish‐kebab structure under the flow field of GAIM was also explored. Copyright © 2012 Society of Chemical Industry     

Extension of the orientation region of high density polyethylene molded by gas‐assisted injection molding: control of the thermal field

Wider zones with close‐knit orientation crystals in high density polyethylene (HDPE) parts prepared via the gas‐assisted injection molding (GAIM) process were obtained under high cooling gas pressure. In this study, compressed nitrogen, as a cooling medium, was introduced to retain a high cooling rate of the polymer melt. The high gas pressure leads to fast cooling of the polymer melt, which contributes to the stability of more oriented and stretched chains during the cooling stage. Then many more oriented structures are formed. SEM shows that many more oriented structures and interlocking shish‐kebab structures are achieved in parts under highest cooling gas pressure (P3). The P3 parts possess a higher degree of orientation than the corresponding regions of parts under lowest cooling gas pressure (P1). Moreover, tensile testing indicates that, compared with P1 parts, although P3 parts have lower crystallinity, the mechanical properties are improved because of the wider orientation zone and many more interlocking shish‐kebab structures. Combining the HDPE molecular parameters with the characteristics of the GAIM flow field and temperature field, the stability of oriented or stretched chains and the formation of orientation structures in various zones of the parts were analyzed. © 2014 Society of Chemical Industry     

Simulations of a full three‐dimensional packing process and flow‐induced stresses in injection molding

Numerical investigations of a full three‐dimensional (3D) packing process and flow‐induced stresses are presented. The model was constructed on the basis of a 3D nonisothermal weakly compressible viscoelastic flow model combined with extended pom‐pom (XPP) constitutive and Tait state equations. A hybrid finite element method (FEM)–finite volume method (FVM) is proposed for solving this model. The momentum equations were solved by the FEM, in which a discrete elastic viscous stress split scheme was used to overcome the elastic stress instability, and an implicit scheme of iterative weakly compressible Crank–Nicolson‐based split scheme was used to avoid the Ladyshenskaya–Babu?ka–Brezzi condition. The energy and XPP equations were solved by the FVM, in which an upwind scheme was used for the strongly convection‐dominated problem of the energy equation. Subsequently, the validity of the proposed method was verified by the benchmark problem, and a full 3D packing process and flow‐induced stresses were simulated. The pressure and stresses distributions were studied in the packing process and were in agreement with the results of the literature and experiments in tendency. We particularly focused on the effects of the elasticity and pressure on the flow‐induced stresses. The numerical results show that normal stress differences decreased with incremental Weissenberg number and increased with incremental holding pressure. The research results had a certain reference value for improving the properties of products in actual production processes. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Super polyolefin blends achieved via dynamic packing injection molding: the morphology and mechanical properties of HDPE/EVA blends

As a part of long-term project aimed at super polyolefin blends, in this work, we report the mechanical reinforcement and phase morphology of the blends of high-density polyethylene (HDPE) and ethylene vinyl acetate (EVA) achieved by dynamic packing injection molding. The shear stress (achieved by dynamic packing injection molding) and interfacial interaction (obtained by using EVA with different VA content) have a great effect on phase morphology and thus mechanical properties. The super HDPE/EVA blends having high modulus (1.9–2.2 GPa), high tensile strength (100–120 MPa) and high impact strength (six times as that of pure HDPE) have been prepared by controlling the phase separation, molecular orientation and crystal morphology of the blends. The phase inversion was also found to shift towards lower EVA content under shear stress. The enhancement of tensile strength and modulus originates from the formation of oriented layer, while the high impact strength is related to shear induced phase morphology. DSC studies indicated that the shish kebab crystal structure that also contributes to the enhancement of tensile strength is formed in the oriented layer. The dramatic improvement of impact strength may result from the formation of microfibers and elongated EVA particles along the flow direction. Wu's toughening theory was found non-applicable for the elongated and oriented rubber particles, and a brittle–ductile–brittle transition was observed with increasing EVA content.     

Mechanical Properties and Crystal Structure of HDPE Induced by Small Amount of High-molecular-weight and Low-molecular-weight Polyethylene under Shear Stress Produced by Dynamic Packing Injection Molding

In order to better understand the effect of small amount of both high-molecular-weight polyethylene (HMWPE) and low-molecular-weight polyethylene (LMWPE) on the mechanical properties and crystal morphology under the shear stress field, the dynamic packing injection molding (DPIM) was used to prepare the oriented pure polyethylene samples and its blends ones with different contents of HMWPE and LMWPE. The experiment substantiated that the further improvement of tensile strength and impact stength along the flow direction (MD) of HDPE/HMWPE/LMWPE samples was achieved, while the tensile strength along the transverse direction (TD) still substantially exceeded that of conventional molding. When the contents of HMWPE and LMWPE were respectively 8% in blends, the tensile strength in both flow and transverse directions of the samples were highly enhanced, with improvements from 27.75 MPa to 115.43 MPa (about 316%), in MD and from 23MPa to 32.74 MPa (about 42.34%), in TD; besides the impact strength was improved from 21.55 KJ/m² to 72.6 KJ/m² (about 236.89%), in MD but decreased from 17 KJ/m² to 6.92 KJ/m² in TD. The obtained samples were characterized via DSC, WAXD and SEM. For HDPE/HMWPE/LMWPE, the shish-kebab structure which is composed of stretched chains (shish) and lamellae (kebab) was seen in the oriented region of DPIM samples and the spherulites existed in the oriented region of SPIM samples. Furthermore, the appropriate amount HMWPE and LMWPE (about 8%, respectively) blended into mixture can improve the thickness and the length of lamellae, and the degree of crystallinity in shear region by DPIM which were approved by DSC and SEM, at the same time, it can also enhance the intensity of orientation of lamellae in shear region confirmed by SEM and WAXD. The reason of improvement of mechanical properties is the existence of these thicker, longer and more orientated lamellae in shear region.     

Study of the effect of organic clay on the shear‐induced crystallization of high‐density polyethylene through dynamic‐packing injection molding

Organic nanoparticles as heterogeneous nucleators have a great effect on the crystallization of polymer matrices in nanocomposite systems, and the effect will be enhanced under shear flow. A home‐made dynamic‐packing injection molding (DPIM) device was developed to explore the effect of organic clay on the shear‐induced crystallization of high‐density polyethylene (HDPE). Differential scanning calorimetry (DSC), wide‐angle X‐ray diffraction (WAXD) and scanning electron microscopy (SEM) were used to characterize the flow‐induced crystalline structure of HDPE/clay nanocomposite injection moldings. It was found that higher crystallinity and thicker crystal planes which contribute to the improvement of mechanical properties were achieved in HDPE/clay nanocomposite samples prepared by DPIM. DSC results clearly showed that an increase of about 16% in crystallinity was achieved in dynamic HDPE/clay nanocomposite samples compared with traditional unfilled HDPE samples. WAXD confirmed that dynamic HDPE/clay nanocomposite samples had maximum crystal sizes at the (110) and (200) planes of 335 and 305 Å, respectively. SEM images indicated that the arrangement of crystalline structures in dynamic HDPE/clay samples was altered slightly compared with unfilled HDPE samples prepared using the same processing parameters. The results showed that organic clay was beneficial for increasing crystallinity and crystal size in the HDPE/clay nanocomposite system under shear flow. Meanwhile the arrangement of crystalline structures was insignificantly affected by the organic clay, and the preferred regular arrangement of lamellae could still be formed in the dynamic HDPE/clay nanocomposite system. Copyright © 2010 Society of Chemical Industry     

Structure development and interfacial interactions in high‐density polyethylene/hydroxyapatite (HDPE/HA) composites molded with preferred orientation

Composites of high‐density polyethylene (HDPE) filled with sintered and nonsintered hydroxyapatite (HA) powders, designated as HAs and HAns, respectively, were compounded by twin screw extrusion. Compounds with neoalkoxy titanate or zirconate coupling agents were also produced to improve interfacial interaction and filler dispersion in the composites. The composites were molded into tensile test bars using (i) conventional injection molding and (ii) shear‐controlled orientation in injection molding (SCORIM). This latter molding technique was used to deliberately induce a strong anisotropic character to the composites. The mechanical characterization included tensile testing and microhardness measurements. The morphology of the moldings was studied by both polarized light microscopy and scanning electron microscopy, and the structure developed was assessed by wide‐angle X‐ray diffraction. The reinforcing effect of HA particles was found to depend on the molding technique employed. The higher mechanical performance of SCORIM processed composites results from the much higher orientation of the matrix and, to a lesser extent, from the superior degree of filler dispersion compared with conventional moldings. The strong anisotropy of the SCORIM moldings is associated with a clear laminated morphology developed during shear application stage. The titanate and the zirconate coupling agents caused significant variations in the tensile test behavior, but their influence was strongly dependent on the molding technique employed. The application of shear associated with the use of coupling agents promotes the disruption of the HA agglomerates and improves mechanical performance. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 2873–2886, 2002     

Improved mechanical properties and structure of PP/nano‐CaCO3 blends prepared by low‐frequency vibration injection molding

BACKGROUD: Melt vibration technology was used to prepare injection samples of polypropylene (PP)/nano‐CaCO₃ blends. It is well known that nano‐CaCO₃ particles are easy to agglomerate owing to their large surface energy. Improving the distribution of nano‐CaCO₃ particles in PP/nano‐CaCO₃ blends is very important for enhancing the mechanical properties. In this work, low‐frequency vibration was imposed on the process of injection molding of PP/nano‐CaCO₃ blends. The aim of importing a vibration field was to change the crystal structure of PP as we studied previously and improve the distribution of nano‐CaCO₃ particles. Furthermore, the mechanical properties were improved. RESULTS: Through melt vibration, the mechanical properties of PP/nano‐CaCO₃ samples were improved significantly. Compared with conventional injection molding, the enhancement of the tensile strength and impact strength of the samples molded by vibration injection molding was 17.68 and 175.96%, respectively. According to scanning electron microscopy, wide‐angle X‐ray diffraction and differential scanning calorimetry measurements, it was found that a much better dispersion of nano‐CaCO₃ in samples was achieved by vibration injection molding. Moreover, the crystal structure of PP in PP/CaCO₃ vibration samples changed. The γ crystal form was achieved at the shear layer of vibration samples. Moreover, the degree of crystallinity of PP in vibration samples increased 6% compared with conventional samples. CONCLUSION: Concerning the microstructure, melt vibration could effectively change the crystal structure and increase the degree of crystallinity of PP besides improving the distribution of nano‐CaCO₃ particles. Concerning the macrostructure, melt vibration could enhance the mechanical properties. The improvement of mechanical properties of PP/nano‐CaCO₃ blends prepared by low‐frequency vibration injection molding should be attributed to the even distribution of nano‐CaCO₃ particles and the formation of γ‐PP and the increase of the degree of cystallinity. Copyright © 2007 Society of Chemical Industry     

Warpage of a large‐sized orthogonal stiffened plate produced by injection molding and injection compression molding

Rectangular plates of the size of 1800 × 600 × 12 mm³ and 1200 × 600 × 12 mm³ were selected for injection molding and injection compression molding, respectively, in order to investigate warpage characteristics of the large‐sized polymer plates with orthogonal stiffener. To determine the mold system and to reduce warpage of the specimen, numerical analyses for injection molding and injection compression molding were performed by using a commercial simulation code. Experiments were performed to verify the suggested mold system and warpage of the specimen. Relatively large warpage of the injection molded product was observed and small warpage of the injection compression molded product was generated. Compression force of the injection compression molding was only 6% of the clamp force of the injection molding. Warpage of the product was reduced significantly by using the injection compression molding. The injection compression molding will be used to substitute expensive and disused wood forms with inexpensive and recyclable polymer plates for concrete casting. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Physical–mechanical properties and morphological study on nylon‐6 recycling by injection molding

The effect of the multiple recycling of nylon‐6 by injection molding on its physical–mechanical properties and morphology was studied after each cycle of injection. These studies were made in order to know how many times it is possible to recycle the nylon‐6 without significant loss of the physical–mechanical properties. Optical and electronic microscopy were used to evaluated the morphology. Molecular weight changes were determinated by gel permeation chromatography (GPC). The nylon‐6 was recycled 10 times, until the eighth cycle the properties of the material did not suffered any change. Changes of 10–15% in the properties between nylon‐6 with 10 cycles of injection and virgin material were observed. An exception was the percentage of elongation that decreased 70% gradually until in the tenth cycle of injection. The results from GPC show that the molecular weight of nylon‐6 increased with recycling (M_w = 17% and M_n = 14%). With the reprocess was also observed the presence of gels. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 851–858, 2000     

Mechanical properties and morphological behavior of calcium carbonate‐filled polypropylene in dynamic injection molding

A custom‐made electromagnetic dynamic injection molding machine was adopted to study the mechanical properties and morphological behavior of calcium carbonate‐filled polypropylene (PP) in a dynamic injection molding process. The influence of vibration amplitude and frequency on the mechanical properties and morphological behavior of samples was investigated using tensile tests, notched Izod impact tests, differential scanning calorimetry, and scanning electronic microscopy. The tensile stress and the impact stress for all samples investigated were found to increase in a nonlinear manner with increasing vibration amplitude and frequency. The tensile stress reached a maximum value at about 8 Hz and 0.15 mm for neat PP and PP filled with 3, 20, and 30 wt% CaCO₃. For PP filled with 40 wt% CaCO₃, the tensile stress reached a maximum value at about 12 Hz and 0.2 mm. The impact stress reached a maximum value at about 12 Hz. From DSC experiments it was shown that the melting temperature slightly increased, but no new polymeric crystalline peak appeared under the vibration force field. The CaCO₃ particles were diffused easily and distributed evenly in the PP melt under the vibration force field, so it is very useful in improving the quality of injection products. Copyright © 2006 Society of Chemical Industry     

Tensile properties in the oriented blends of high-density polyethylene and isotactic polypropylene obtained by dynamic packing injection molding

In this article, tensile properties have been discussed in terms of phase morphology, crystallinity and molecular orientation in the HDPE/iPP blends, prepared via dynamic packing injection molding, with aid of scanning electron microscopy (SEM), differential scanning calorimetry (DSC) as well as two dimensional X-ray scattering (2D WAXS). For the un-oriented blends, the tensile properties (tensile strength and modulus) are mainly dominated by the phase morphology and interfacial adhesion related to the influenced crystallization between HDPE and iPP component. A maximum in tensile strength and modulus is found at iPP content in the range of 70-80 v/v%. As for the oriented blends, however, the presence of dispersed phase in the blends, independent of phase morphology and crystallinity, always makes tensile properties to be deteriorated through reducing molecular orientation of matrix. It is molecular orientation of matrix that determines the tensile properties of oriented blends. In the blends with HDPE as matrix, steep decreasing of tensile properties is related to the rapid reducing of molecular orientation of HDPE, whereas in the blends with iPP as a major component, slight decreasing of molecular orientation of iPP results in slight reducing of tensile properties. Other factors, such as interfacial properties and phase morphology, seem to be little contribution to the modulus and tensile strength.     

Morphology and mechanical properties of injection‐molded ultrahigh molecular weight polyethylene/polypropylene blends and comparison with compression molding

The mechanical properties and morphology of UHMWPE/PP(80/20) blend molded by injection and compression‐molding were investigated comparatively. The results showed that the injection‐molded part had obviously higher Young's modulus and yield strength, and much lower elongation at break and impact strength, than compression‐molded one. A skin‐core structure was formed during injection molding in which UHMWPE particles elongated highly in the skin and the orientation was much weakened in the core. In the compression‐molded part, the phase morphology was isotropic from the skin to the core section. The difference in consolidation degree between two molded parts that the compression molded part consolidated better than the injection one was also clearly shown. In addition, compositional analysis revealed that there was more PP in the skin than core for the injection‐molded part, whereas opposite case occurred to the compression‐molded one. All these factors together accounted for the different behavior in mechanical properties for two molded parts. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Mechanical properties and structure of high‐density polyethylene samples prepared by injection molding with low‐frequency vibration

To better understand the formation of different crystal structures and improve the mechanical properties of high‐density polyethylene samples, melt vibration technology, which generally includes shear vibration and hydrostatic pressure vibration, was used to prepare injection samples. Through melt vibration, the crystal structure changed from typical spherulites of the traditional injection sample to obviously orientated lamellae of vibration samples. Sizes and orientation degrees of lamellae were different according to different vibration conditions. Crystallinity degrees of vibration samples increased notably. Therefore, the tensile strength of vibration samples increased with increasing vibration frequency and vibration pressure, whereas elongation of vibration samples decreased during the first stage and then continued to increase as the vibration frequency increased. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 818–823, 2005