Compounding and injection molding of polybutene‐1/polypropylene blends

The effect of shear‐controlled orientation injection molding (SCORIM) was investigated for polybutene‐1/polypropylene blends. This article reports on the methods and processing conditions used for blending and injection molding. The properties of SCORIM moldings are compared with those of conventional moldings. SCORIM is based on the application of specific macroscopic shears to a solidifying melt. The multiple shear action enhances molecular alignment. The moldings were investigated with mechanical tests, differential scanning calorimetry studies, and polarized light microscopy. The application of SCORIM improved Young's modulus and the ultimate tensile strength. The gain in stiffness was greater for higher polybutene‐1 content blends. A drastic decrease in the strain at break and toughness was observed in SCORIM moldings. The enhanced molecular orientation of SCORIM moldings resulted in a featureless appearance of the morphology. Interfacial features due to segregation were visible in the micrographs of SCORIM moldings. Both conventional and SCORIM moldings exhibited form I′ in polybutene‐1. This article explains the relationship between the mechanical properties and micromorphologies. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 806–813, 2003     

The enhancement of the mechanical properties of a high-density polyethylene

This paper describes the process optimization in injection molding of high-density polyethylene (HDPE). Both conventional injection molding and shear controlled orientation (SCORIM) were employed in processing. The process optimization was based on design of experiments and complemented with analysis of variance. Mechanical characterization was carried out by tensile testing. Wide-angle X-ray diffraction and differential scanning calorimetry were used for the structural characterization of the moldings. High-density polyethylene exhibits 7.2 GPa Young's modulus and 155 MPa of ultimate tensile strength following the application of SCORIM processing. These results account for a fourfold increase in Young's modulus and a fivefold increase in ultimate tensile strength compared to conventional injection molding. The maintenance of toughness while enhancing stiffness and strength of the SCORIM moldings is attributable to an oriented morphology developed during shear flow, i.e., shish-kebab structure. The frequency of shearing action has the strongest influence on the morphology development. It is also demonstrated that the studied parameters are very much interdependent. It is possible to achieve substantial gains in mechanical properties of HDPE in SCORIM processing without causing a substantial increase in cycle time. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2473–2483, 1999     

Mechanical performance of starch based bioactive composite biomaterials molded with preferred orientation

Composites of blends of starch with ethylene vinyl alcohol copolymer (SEVA‐C) filled with 10, 30 and 50% by weight (wt.) of hydroxyapatite (HA–the major inorganic constituent of human bone) were produced by twin‐screw extrusion (TSE) compounding. These composites were molded into tensile test bars using two molding techniques: (i) conventional injection molding and (ii) shear controlled orientation in injection molding (SCORIM). The bars produced were mechanically characterized by means of tensile testing and dynamical mechanical analysis (DMA). The structure of the moldings was assessed by wide‐angle X‐ray diffraction (WAXD) and the failure surfaces of the moldings analyzed by scanning electron microscopy (SEM). The enhancement of stiffness observed with HA reinforcement results partially from the stiffening effect of the blend associated with the decrease in plasticizer content during the compounding stage. SCORIM was able to further increase the stiffness of SEVA‐C/HA composites, allowing a maximum improvement of 12% for 30% wt. HA as compared to conventional molding. DMA results showed that the reinforcement of SEVA‐C causes the broadening of the relaxation peak of the polymer, suggesting a structural change within the starch fraction that may be related with thermal degradation of the polymer. The addition of HA particles reduces the preferred orientation exhibited by the SEVA‐C matrix, which is believed to limit the maximum mechanical performance that can be attained. Nevertheless, composites based on a biodegradable matrix with modulus above 7 GPa (in the bounds of the lower limit for human cortical bone) could be successfully produced.     

Injection molding of a starch/EVOH blend aimed as an alternative biomaterial for temporary applications

Biodegradable polymers show great potential to be used as materials for temporary implants and bone replacement applications in orthopedics. However, its use in high load‐bearing applications will depend on the successful development of biodegradable implants with a mechanical performance matching that of human bone. This article describes the optimization of the injection molding process of an alternative biodegradable starch‐based polymer aimed at biomedical applications. A blend of starch with a copolymer of ethylene–vinyl alcohol (SEVA‐C) was studied. Both conventional injection molding and shear controlled orientation (SCORIM) were optimized with the support of design of experiments and analysis of variance techniques. The mechanical characterization was performed by tensile testing. The structure developed within the moldings was assessed by wide‐angle X‐ray diffraction and differential scanning calorimetry. Increases up to 30% in the tangent modulus and 20% in the ultimate tensile strength compared with conventional molding were achieved with the application of SCORIM. The holding pressure and the frequency of the shear applied have the strongest influence on the morphology development and consequently on the mechanical performance. The solidification of SEVA‐C at high cavity pressures enhances stiffness for long durations of the shearing stage in SCORIM. However, the effect of viscous heating of SEVA‐C is important and ought to be considered. A decrease of the material phase miscibility in SEVA‐C occurs as result of the shear fields imposed. The microstructure evaluation suggests that the mechanical properties enhancement in SCORIM molded SEVA‐C is attributable to preferred orientation developed during processing. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 1303–1315, 2000     

Structure and physical property relationships in processed polybutene‐1

The effect of SCORIM was investigated on three grades of polybutene‐1 and one grade of ethylene–butene‐1 copolymer. The methods and processing conditions used for injection molding and the properties of the moldings are reported. Phase transformations and their relationship with mechanical properties are discussed in detail. Both, conventional and shear‐controlled orientation injection molding (SCORIM) were employed to produce moldings. SCORIM is based on the application of specific macroscopic shears to a solidifying melt. The multiple shear action enhances molecular alignment. The moldings were investigated by performing mechanical tests, fractographic analysis, differential scanning calorimetry studies, wide‐angle X‐ray diffraction, polarized light microscopy, and atomic force microscopy. The application of SCORIM improves the mechanical performance. Molecular orientation results in the formation of shish‐kebab morphology. One grade of polybutene‐1 exhibited a greater than fivefold increase in Young's modulus. The application of high cavity pressures favored the formation of the stable Form I' in polybutene‐1. The formation of Form I' led to a decrease in crystallinity and mechanical properties. However, this loss was by far smaller than the gain obtained via the formation of shish‐kebab morphology. The relationship between mechanical properties and micromorphologies of the investigated materials is explained. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 814–824, 2003     

Structural development of HDPE in injection molding

This study investigated some relevant structure/properties relationships in shear‐controlled orientation in injection molding (SCORIM) of high‐density polyethylene (HDPE). SCORIM was used to deliberately induce a strong anisotropic character in the HDPE microstructure. Three grades with different molecular weight characteristics were molded into tensile test bars, which were subsequently characterized in terms of the mechanical behavior by tensile tests and microhardness measurements. The structure developed upon processing was also characterized by polarized light microscopy (PLM), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and wide‐angle X‐ray diffraction (WAXD). SCORIM allows the production of very stiff molded parts, exhibiting a very well‐defined laminated morphology. This morphology is associated with both an M‐shaped microhardness profile and a pronounced mechanical anisotropy. These characteristics are supported by an analogous variation in the crystallinity and a high level of molecular orientation, as indicated, respectively, by calorimetric measurements and X‐ray diffraction results. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2079–2087, 2003     

Injection‐molded high‐density polyethylene–hydroxyapatite–aluminum oxide hybrid composites for hard‐tissue replacement: Mechanical,biological, and protein adsorption behavior

In this article, we report the mechanical and biocompatibility properties of injection‐molded high‐density polyethylene (HDPE) composites reinforced with 40 wt % ceramic filler [hydroxyapatite (HA) and/or Al₂O₃] and 2 wt % titanate as a coupling agent. The mechanical property measurements revealed that a combination of a maximum tensile strength of 18.7 MPa and a maximum tensile modulus of about 855 MPa could be achieved with the injection‐molded HDPE–20 wt % HA–20 wt % Al₂O₃ composites. For the same composite composition, the maximum compression strength was determined to be 71.6 MPa and the compression modulus was about 660 MPa. The fractrography study revealed the uniform distribution of ceramic fillers in the semicrystalline HDPE matrix. The cytocompatibility study with osteoblast‐like SaOS2 cells confirmed extensive cell adhesion and proliferation on the injection‐molded HDPE–20 wt % HA–20 wt % Al₂O₃ composites. The cell viability analysis with the 3(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assay revealed a statistically significant difference between the injection‐molded HDPE–20 wt % HA–20 wt % Al₂O₃ composites and sintered HA for various culture durations of upto 7 days. The difference in cytocompatibility properties among the biocomposites is explained in terms of the difference in the protein absorption behavior. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Mica reinforced nylon‐6: Effect of coupling agents on mechanical,thermal, and dielectric properties

The effects of applying titanate (TYZOR® TPT) and silane (DYNASYLAN VTMO) coupling agents to wet ground muscovite mica in nylon‐6 composites are described. Nylon‐6 composites of 5–40 wt % filler loadings were compounded using an APV Baker twin‐screw extruder. Mica (25 wt %) brought about an increase in the Young's modulus, flexural strength, and flexural modulus but did not produce significant variations in tensile and impact strength. Hence different coupling agents were employed. It was observed that titanate coupling agent improved the tensile strength and the Young's modulus of the composites much while the impact properties were enhanced by the silane coupling agent. An attempt was made to use ?‐caprolactum in improving the interfacial adhesion of the filler and the matrix. It was observed that ?‐caprolactum improved the flexural modulus of the composites most. The effect of coupling agents on the dielectric strength, heat distortion temperature, and morphology were also investigated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4074–4081, 2006     

Shear‐induced crystallization of injection molded vetiver grass‐polypropylene composites

Vetiver grass was used as an alternative filler in polypropylene (PP) composites in this study. Chemical treatment of vetiver grass by alkalization was carried out to obtain alkali‐treated vetiver grass. It was shown that alkali‐treated vetiver grass exhibited higher thermal stability than untreated vetiver grass. Injection molding was used to prepare the composites. The microstructure of injection molded samples showed a distinct skin layer due to shear‐induced crystallization. It was found that normalized thickness of shear‐induced crystallization layer of the composite was lower than that of neat PP. The effect of vetiver particle sizes on shear‐induced crystallization and physical properties of the composites were elucidated. Furthermore, the effect of processing conditions on shear‐induced crystallization, degree of crystallinity, gapwise crystallinity distribution, and mechanical properties of the composite were investigated. It was shown that injection speed and mold temperature affected the normalized thickness of shear‐induced crystallization layer and degree of crystallinity of the composites. However, processing conditions showed insignificant effect on the mechanical properties of vetiver fiber‐PP composites. The degree of crystallinity showed no distribution throughout the thickness direction of the composites. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

PVDF-based composites containing PZT particles: How processing affects the final properties

Poly(vinylidene fluoride) (PVDF)-based composites containing up to 30 vol % of lead zirconate titanate (PZT) particles were prepared by: (a) different techniques, melt blending and solvent casting; and (b) different molding procedures, a single-step and a two-step hot-pressing method. The obtained samples were characterized in order to study how the processing affects their final properties. Results indicate that the different molding processes have a strong effect on polymorphism and molecular relaxations of PVDF as well as on dielectric response of the composite materials, that results enhanced by the two-step molding. The preparation technique influences the filler dispersion and, consequently, the elastic modulus of the composites, but without remarkably impacting on other properties. This suggests the possibility of preparing performing composites by a solvent-free and easily scalable technique (i.e., melt blending) and obtaining suitable dielectric characteristics, very important for application of such kind of materials, just by tuning the molding conditions. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48871.     

Shear Enhanced Fiber Orientation and Adhesion in PP/Glass Fiber Composites

Summary: In order to achieve better mechanical properties, most work on polymer/fiber composites has been focused on the importance of the chemistry used to modify the surface of the fibers and improving the adhesion between the fiber and the matrix using coupling agents. Our purpose in this study was to determine the effect of shear on the fiber orientation and interfacial adhesion in poly(propylene)/glass fiber composites via dynamic packing injection molding (DPIM), in which the melt is first injected into the mold and then forced to move repeatedly in a chamber by two pistons that move reversibly with the same frequency as the solidification progressively occurs from the mold wall to the molding core part. SEM, TGA, FT‐IR, AFM and mechanical testing were used to characterize the samples obtained. The majority of fibers are aligned parallel to the flow direction along the sample thickness, even at the core, in contrast to the products obtained via conventional injection molding where the orientation of fibers is observed only at the skin. More importantly, we found that shear could enhance not only the fiber orientation, but also the interfacial adhesion between the fibers and the matrix, particularly for samples with higher fiber contents, resulting in an obvious increase in tensile strength and the onset degradation temperature. A possible transcrystallization was evidenced by AFM investigations of the dynamic packing injection molded samples, which is worth further study.

SEM micrographs representing the glass fiber after PP in the composites was extracted (GF30, dynamic sample).     

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     

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     

Effects of a titanate coupling agent on the mechanical and thermo‐physical properties of talc‐reinforced polyethylene compounds

An experimental study was carried out to investigate the effects of a titanate coupling agent on the mechanical properties, moisture absorption, and thermal conductivity of talc‐filled high‐density polyethylene (HDPE). Talc (0–35 wt %) was used as reinforcement particulate filler in an HDPE matrix and samples were prepared in a micro‐compounder and an injection molding machine. Isopropyl tri(dioctyl)phosphate titanate (0.5 wt %) was used as coupling agent. Composites with and without coupling agent were evaluated for changes in mechanical and thermo‐physical properties, morphology, and void content. Addition of the titanate coupling agent most often resulted in an increase in stiffness and tensile strength. Furthermore, both the void content and the elongation at break of composites were reduced. Results also showed that the coupling agent had no effects on the thermal conductivity, thermal diffusivity, and specific heat capacity of the composites. In addition, it was observed that the coupling agent was more effective at low concentrations of filler. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40449.     

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     

Effects of a coupling agent on the mechanical and thermal properties of ultrahigh molecular weight polyethylene/nano silicon carbide composites

Ultra‐high‐molecular‐weight polyethylene (UHMWPE)/nano silicon carbide (nano‐SiC) composites were prepared by compression molding. The effects of a coupling agent and the content of the filler on the filler dispersion and the mechanical and thermal properties of the composites were investigated. The results show that the mechanical properties of the composites first increased and then decreased with increasing SiC content. The macromolecular coupling agent exhibited a much better reinforcing effect than the small‐molecule coupling agent. The tensile strength of the composites with 3‐aminopropyltriethoxysilane (KH550), γ‐methacryloxypropyltrimethoxysilane (KH570), and silicone powders reached its maximum value when the silicon carbide (SiC) content was 3%. We found that a web of the UHMWPE/SiC/coupling agent was formed and played a significant role in improving the heat resistance of the composites. In addition, appropriate amounts of SiC could increase the crystallinity of UHMWPE via a process of heterogeneous nucleation. The comprehensive performance of the KH550/silicone/SiC/UHMWPE composites was the best. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

动态注射成型短玻纤增强高密度聚乙烯力学性能的研究

在不同的振动条件下注射成型短玻纤增强高密度聚乙烯复合材料。实验表明,振动可以有效地改善玻纤在树脂基体中的分散取向状况,提高复合材料的力学性能。与稳态注射成型的复合材料相比,动态注射成型复合材料的拉伸强度最大可提高11.1%,冲击强度最大可提高11.4%。     

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     

Morphology of gas‐assisted and conventional injection molded polycarbonate/polyethylene blend

The skin‐core structure of the gas‐assisted and conventional injection molded polycarbonate (PC)/polyethylene (PE) blend was investigated. The results indicated that both the size and the shape of the dispersed PC phase depended not only on the nature of PC/PE blend and molding parameters, but also on its location in the parts. Although the gas‐assisted injection molding (GAIM) parts and conventional injection molding (CIM) part have the similar skin‐core structure, the morphology evolution of PC phase in the GAIM moldings and the CIM moldings showed completely different characteristics. In the section perpendicular to the melt flow direction, the morphology of the GAIM moldings included five layers, skin intermediate layer, subskin, core layer, core intermediate layer as well as gas channel intermediate layer, according to the degree of deformation. PC phase changed severely in the core layer of GAIM moldings, as well as in the subskin of CIM moldings. In GAIM parts, PC phase in the core layer of the nongate end changed far more intensely and aligned much orderly than that in the gate end. The morphology of PC phase in the GAIM part molded with higher gas pressure changed more severe than that in the GAIM part molded with lower gas pressure. In a word, PC phase showed more obvious fibrillation in the GAIM moldings than that in the CIM moldings. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 3069–3077, 2006     

Mechanical and morphological properties of white rice husk ash filled polypropylene/ethylene‐propylene‐diene terpolymer thermoplastic elastomer composites

The performance of white rice husk ash (WRHA) as filler for polypropylene (PP)/ethylene‐propylene‐diene terpolymer (EPDM) thermoplastic elastomer (TPE) composites was investigated. The composites with different filler loadings were prepared in a Brabender plasticorder internal mixer. Both unvulcanized and dynamically vulcanized composites were prepared. Mixing and vulcanization processes of the composites were monitored through the typical Brabender torque‐time curves. The mechanical properties and morphology of the composites were also studied. The Brabender torque curves revealed that the dynamic vulcanization process employed was successful and incorporation of filler has no adverse effect on the processibility of the composites. Incorporation of WRHA improves the tensile modulus and flexural modulus and lowers tensile strength, elongation at break, tear strength, and toughness of both types of composites. Dynamic vulcanization significantly enhances the mechanical and TPE properties of the composites. Dynamic mechanical analysis (DMA) study revealed the existence of two phases in both types of composites. It further shows that neither dynamic vulcanization nor filler agglomeration has played a prominent role in the compatibility of the composites. Thermogravimetric investigation shows that dynamic vulcanization or WRHA loading has not adversely affected the thermal stability of the composites. The scanning electron micrographs provide evidence for the tendency to form filler agglomerates with increasing filler loading, better filler dispersion of dynamically vulcanized composites over unvulcanized composites, and effective vulcanization of elastomer phase of the composites in the presence of filler. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 438–453, 2002