Dynamic rheological properties of high‐density polyethylene/polystyrene blends extruded in the presence of ultrasonic oscillations

The linear rheological properties of high‐density polyethylene (HDPE), polystyrene (PS), and HDPE/PS (80/20) blends were used to characterize their structural development during extrusion in the presence of ultrasonic oscillations. The master curves of the storage shear modulus (G′) and loss shear modulus (G″) at 200°C for HDPE, PS, and HDPE/PS (80/20) blends were constructed with time–temperature superposition, and their zero shear viscosity was determined from Cole–Cole plots of the out‐of‐phase viscous component of the dynamic complex viscosity (η″) versus the dynamic shear viscosity. The experimental results showed that ultrasonic oscillations during extrusion reduced G′ and G″ as well as the zero shear viscosity of HDPE and PS because of their mechanochemical degradation in the presence of ultrasonic oscillations; this was confirmed by molecular weight measurements. Ultrasonic oscillations increased the slopes of log G′ versus log G″ for HDPE and PS in the low‐frequency terminal zone because of the increase in their molecular weight distributions. The slopes of log G′ versus log G″ for HDPE/PS (80/20) blends and an emulsion model were used to characterize the ultrasonic enhancement of the compatibility of the blends. The results showed that ultrasonic oscillations could reduce the interfacial tension and enhance the compatibility of the blends, and this was consistent with our previous work. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 3153–3158, 2004     

Thermal and mechanical properties for binary blends of metallocene polyethylene with conventional polyolefins

The thermal and mechanical properties for four binary blends, high-density polyethylene (HDPE)–metallocene polyethylene (MCPE), polypropylene (PP)–MCPE, poly(propylene-co-ethylene) (CoPP)–MCPE, and poly(propylene-co-ethylene-co-1-butene) (TerPP)–MCPE were investigated to compare the compatibility and molecular micromechanism of the blends. We report in this work all the blend systems that are thermodynamically immiscible but mechanically compatible which have been understood by their thermal and mechanical behaviors. A lower content of MCPE (up to 50%) in PP–MCPE, CoPP–MCPE, and TerPP–MCPE blends showed discernibly two β transitions, whereas β relaxation was shifted to a lower temperature with the MCPE content in the HDPE–MCPE system. These results conclude that the degree of compatibility in the HDPE–MCPE blend is the largest among the blend systems that we have studied, which also can be explained in terms of the similar chemical structure of polyolefins. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 2441–2450, 1998     

A polypropylene/high density polyethylene blend compatibilized with an ethylene‐propylene‐diene monomer block copolymer: Fitting dynamic rheological data by emulsion models with a physical scheme

The dynamic rheological behaviors at 210, 230, and 250 °C are measured by small amplitude oscillatory shear on a rotational rheometer for a polypropylene(PP)/ ethylene‐propylene‐diene monomer(EPDM) block copolymer/ high density polyethylene (HDPE)/blend. The scanning electron microscope (SEM) photomicrographs show the blend has a droplet/matrix, semi‐co‐continuous, co‐continuous morphology respectively at different weight ratios. The Cole–Cole (G″ vs. G′) data of the blends can be fitted by the simplified Palierne's model only for very narrow weight ratios. A physical scheme is proposed that the dispersed droplets are enclosed by EPDM, thus an equivalent dispersed phase is made up of “expanded” EPDM. With this physical scheme the G″ vs. G′ data of the HDPE‐rich blends at 210 °C can be fitted well by Palierne's model. Also with the physical scheme the G″ vs. G′ data of the PP‐rich blends at three temperatures can be fitted well by G–M's model with G* of interface equals to zero. This means the proposed physical scheme is reasonable. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43709.     

Effect of core‐shell morphology evolution on the rheology,crystallization, and mechanical properties of PA6/EPDM‐g‐MA/HDPE ternary blend

In this article, polyamide 6 (PA6), maleic anhydride grafted ethylene‐propylene‐diene monomer (EPDM‐g‐MA), high‐density polyethylene (HDPE) were simultaneously added into an internal mixer to melt‐mixing for different periods. The relationship between morphology and rheological behaviors, crystallization, mechanical properties of PA6/EPDM‐g‐MA/HDPE blends were studied. The phase morphology observation revealed that PA6/EPDM‐g‐MA/HDPE (70/15/15 wt %) blend is constituted from PA6 matrix in which is dispersed core‐shell droplets of HDPE core encapsulated by EPDM‐g‐MA phase and indicated that the mixing time played a crucial role on the evolution of the core‐shell morphology. Rheological measurement manifested that the complex viscosity and storage modulus of ternary blends were notable higher than the pure polymer blends and binary blends which ascribed different phase morphology. Moreover, the maximum notched impact strength of PA6/EPDM‐g‐MA/HDPE blend was 80.7 KJ/m² and this value was 10–11 times higher than that of pure PA6. Particularly, differential scanning calorimetry results indicated that the bulk crystallization temperature of HDPE (114.6°C) was partly weakened and a new crystallization peak appeared at a lower temperature of around 102.2°C as a result of co‐crystal of HDPE and EPDM‐g‐MA. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

The linear viscoelastic behaviors of Nylon1212 blends toughened with elastomer

The linear viscoelastic behaviors of nylon1212 blends toughened with (styrene‐[ethylene‐(ethylene‐propylene)]‐styrene block copolymer) (SEEPS) elastomer were carried out. The results show that dynamic storage modulus (G′) curves of the blends are located between those of virgin nylon and SEEPS within the frequency (ω) tested, and the G′ of blends increases with increasing of the SEEPS content. Moreover, the predictive results of Palierne emulsion model show that it is unsuitable for describing the viscoelastic behaviors of the double phase systems toughened with elastomer, especially for the system with high content of elastomer. The positive deviation in the plots of G′ vs. blend composition demonstrates that the blends are immiscible. From the point of phase transition, the phase inversion region for these blends was predicted to be in the range of 30–50 wt % of SEEPS, which agrees with the morphology analysis of nylon1212/SEEPS blends. In addition, “Cole–Cole” plots of modulus at different temperatures show that the microstructures of blends are unstable in the phase transition region. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Rheological and Mechanical Properties of LDPE/HDPE Blends

Melt rheology and mechanical properties of binary blend of low-density polyethylene (LDPE) and high-density polyethylene (HDPE) have been investigated. Four different wt fractions of blends containing LDPE/HDPE (20/80, 40/60, 60/40, and 80/20) were prepared. Cole-Cole plots [storage melt viscosity (η′) vs. loss melt viscosity (η″)] and relation between storage melt viscosity (η′) with frequency (ω) and blend composition were constructed. Miscibility of blends was established from rheological data. Impact strength of the blends increased with increasing LDPE concentration, whereas tensile strength shows the opposite trends. Percentages of the crystallinity of the blends were calculated by both the differential scanning calorimetry and wide-angle X-ray scattering methods, which show that the percentage of crystallinity decreased with increasing LDPE concentration, but the rate of crystallization of HDPE phase was unaffected.     

Rheological behavior and processability of polypropylene blends with rubber ethylene propylene diene terpolymer

A study of the dynamic complex and steady shear viscosity of isotactic polypropylene (iPP), ethylene–propylene diene terpolymer rubber (EPDM) and three different blends of both polymers are presented over a range of temperatures and frequencies. Moreover, the processability of these materials is studied through torque measurements during blend mixing. The results obtained show that the viscosity gradually increases with rubber content in the blend and decreases with both temperature and frequency. Plots of η″ versus η′ (Cole–Cole plots) show that the blend with the lower rubber content (25%), has a certain rheological compatibility with neat PP. Furthermore, torque curves measured during blend mixing confirm these results, demonstrating that the blend with 25% of elastomer has a similar behavior of iPP during processing. To analyze the morphological structure of the blends, a dynamic mechanical analysis of the solid state is also presented. It is observed that the blends have two distinct values of T_g close to the corresponding values of the pure polymers, confirming that this type of blends based on a semicrystalline polymer and an amorphous elastomer forms a two‐phase system with a limited degree of miscibility between both components. In addition, the polymer present with the higher concentration forms the continuous phase and controls the rheological properties of the blend. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 1–10, 2001     

i-PP/HDPE blends. III. Characterization and compatibilization at lower i-PP contents

The mechanical properties of high-density polyethylene (HDPE)-rich i-PP/HDPE blends were studied. Two grades of HDPE were investigated, one with a melt viscosity close to that of the polypropylene (PP) and the other having a much lower melt viscosity. Compatibilization of the 10/90 i-PP/HDPE blend with three copolymers (an ethylene/propylene/diene [EPDM] copolymer and two ethylene/vinylacetate [EVA] copolymers, differing in their VA content) was also investigated. Blends of PP with the low melt viscosity HDPE displayed poor mechanical properties. It was not possible to improve these properties sufficiently with EPDM or EVA. In the case where viscosity matching was achieved between PP and HDPE, addition of i-PP (up to 30%) to HDPE resulted in a large drop in the impact strength of the blends, compared to that of the neat HDPE. A large drop (>50%) was also observed in the ultimate tensile elongation. However, the flexural modulus, yield stress, and ultimate tensile strength all increased with the introduction of i-PP into HDPE. Modification of these blends with an EPDM resulted in the return of all properties to values very close to those of the neat HDPE. The ultimate tensile elongation of the EPDM-modified i-PP/HDPE blend even exceeded that of the virgin HDPE. It was also found that although EVAs can be used to compatibilize these blends these additives were not as effective as was the EPDM. © 1996 John Wiley & Sons, Inc.     

Crystallization kinetics and tensile modulus of blends of metallocene short‐chain branched polyethylene with conventional polyolefins

In this study, blends of metallocene short‐chain branched polyethylene (SCBPE) with low‐density polyethylene (LDPE), high‐density polyethylene (HDPE), polystyrene (PS), ethylene–propylene–diene monomer (EPDM), and isotactic polypropylene (iPP) were prepared in weight proportions of 80 and 20, respectively. The crystallization behaviors of these blends were studied with polarized light microscopy (PLM) and differential scanning calorimetry. PLM showed that SCBPE/LDPE, SCBPE/HDPE, and SCBPE/EPDM formed band spherulites whose band widths and sizes were both smaller than that of pure SCBPE. No spherulites were observed, but tiny crystallites were observed in the completely immiscible SCBPE/PS, and the crystallites in SCBPE/iPP became smaller; only irregular spherulites were seen. The crystallization kinetics and mechanical properties of SCBPE were greatly affected by the second polyolefin but in different way, depending on the phase behavior and the moduli of the second components. SCBPE may be phase‐miscible in the melt with LDPE, HDPE, and EPDM but phase‐separated during crystallization. A big change in the crystal morphology and crystallization kinetics existed in the SCBPE/iPP blend. The mechanical properties of the blends were also researched with dynamic mechanical analysis (DMA). DMA results showed that the tensile modulus of the blends had nothing to do with the phase behavior but only depended on the modulus of the second component. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 1816–1823;2005     

Dynamic shear rheological behavior of PP/EPR in‐reactor alloys synthesized by multi‐stage sequential polymerization process

The rheological behavior, morphology, and mechanical properties of in‐reactor alloy of polypropylene (PP)/ethylene propylene rubber (EPR) synthesized by multi‐stage sequential polymerization process are studied in this article. The relationship between polymerization parameters, morphology, and rheological properties are evaluated by scanning electron microscopy (SEM) and small amplitude oscillation rheometry in the linear viscoelastic region. The electron microscopy of samples is showed that by increasing switching frequency in polymerization time, the size of EPR particles decrease. By increasing switching frequency, the curves of complex viscosity against angular frequency of samples are shifted to higher values at low range of shear rates with no significant change at higher frequencies in Power‐law region. The modified Cole‐Cole plots revealed the enhanced melt elasticity by increasing switching frequency up to 230°C. The plot of phase angle versus absolute value of complex modulus G* is used for the evaluation of matrix‐droplets interaction at various temperatures. It is observed two different behaviors before and after 230°C which is the evidence of the change in relaxation mechanism of the blend components because of coarsening the rubber particles in the phase separation process. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

In situ fiber composites based on metallocene polyethylene matrices

Binary blends of metallocene polyethylenes with polyethylenes and polypropylene were made in a co‐rotating twin‐screw extruder. A stretching process was carried out afterwards in the melt state at the extruder's exit to study the effect of the induced orientation on their thermal and tensile properties. Capillary rheometry was performed to the neat polymers to determine the viscosity ratios of the blend components as a function of the shear rate. SEM and Micro‐Raman analyses were done to study the morphology of the stretched and nonstretched blends. As expected, an increase in the modulus and tensile stress was obtained through blending. Additionally, the elastomeric behavior of the metallocene polyethylene (mPE) sample is observed in all blends and it was not lost through blending. Nevertheless, all blends without stretching exhibited a negative deviation of the linear additivity rule of blending. The stretching of the blends made with metallocene polyethylenes as matrices and other types of PEs as dispersed phase did not improve the tensile properties, although some differences in the dispersed phases were found by DSC, and microfibrils could be seen in the drawn mPE/HDPE blend. However, blending with PP produced an improvement in the modulus and tensile stress of the drawn samples in comparison to their undrawn counterpart. The tensile stresses of PP blends are more sensitive to the drawing process than the modulus, which can be attributed to the appearance of large fibril fractions during this process. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Mechanical characterization of toughened polyamide‐6 blends with metallocene copolymers

The effectiveness as impact modifier of two in situ maleated metallocene copolymers, a metallocene polyethylene, (mPE1) and a metallocene ethylene‐propylene (mEPDM) and three commercial maleated copolymers (mPE2‐g‐MA, EPDM‐g‐MA, and mEPR‐g‐MA) were studied in binary and ternary blends carried out in an intermeshing corotating twin‐screw extruder with polyamide‐6 (PA) as matrix (80 wt %). Also, the effects of the grafting degree, viscosity ratio, and crystallinity of the dispersed phases on the morphological and mechanical properties of the blends were investigated. A significant improvement of the compatibility of these grafted copolymers with PA6 was shown by FTIR spectroscopy, capillary rheometry, and scanning electron microscopy (SEM) in all reactive blends. The tensile strength values of the mEPR‐g‐MA/PA2 binary blend showed the highest strain hardening. The results obtained in this work indicated that the effectiveness of the grafted copolymers as impact modifier depends on the morphology of the blends and a combination of tensile properties of the blend components such as Young's modulus, Poisson ratio, and break stress. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Study on morphology of ternary polymer blends. I. Effects of melt viscosity and interfacial interaction

The morphology of some ternary blends was investigated. In all of the blends polypropylene, as the major phase, was blended with two different minor phases, ethylene–propylene–diene terpolymer (EPDM) or ethylene–propylene–rubber (EPR) as the first minor phase and high‐density polyethylene (HDPE) or polystyrene (PS) as the second minor phase. All the blends were investigated in a constant composition of 70/15/15 wt %. Theoretical models predict that the dispersed phase of a multiphase polymer blend will either form an encapsulation‐type phase morphology or phases will remain separately dispersed, depending on which morphology has the lower free energy or positive spreading coefficient. Interfacial interaction between phases was found to play a significant role in determining the type of morphology of these blend systems. A core–shell‐type morphology for HDPE encapsulated by rubber was obtained for PP/rubber/PE ternary blends, whereas PP/rubber/PS blends showed a separately dispersed type of morphology. These results were found to be in good agreement with the theoretical predictions. Steady‐state torque for each component was used to study the effect of melt viscosity ratio on the morphology of the blends. It was found that the torque ratios affect only the size of the dispersed phases and have no appreciable influence on the type of morphology. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 1129–1137, 2001     

Influence of crosslinking on crystallization,rheological, and mechanical behaviors of high density polyethylene/ethylene‐vinyl acetate copolymer blends

High density polyethylene (HDPE)/ethylene‐vinyl acetate copolymer (EVA) blends with selective crosslinking the EVA phase were prepared and the crystallization, rheological, and mechanical behaviors were studied. Selective crosslinking of EVA component could greatly improve both tensile and impact strengths of the HDPE‐rich blends and influence melting enthalpy at different annealing temperature in successive self‐nucleation and annealing procedure. Dynamic mechanical analysis reveals that glass transition temperatures of both the HDPE and EVA components are lowered upon blending and are raised upon crosslinking. The uncrosslinked HDPE/EVA blends are unstable in the melt and show increment in storage modulus (G′) and decay in loss tangent (tanδ) with annealing time associated with phase coarsening. However, morphology of selectively crosslinked blends in the melt state is highly unstable, characterized by a fast migration of uncrosslinked HDPE component out of the crosslinked EVA phase to the surface resulting in a rapid decay in G′ and an increment in tanδ at the early stage of annealing. POLYM. ENG. SCI., 54:2848–2858, 2014. © 2014 Society of Plastics Engineers     

Rheological behavior of high‐density polyethylene (HDPE) filled with paper mill sludge

A comparative study was conducted of composites made with sludge from three different paper mills. Sludges were obtained from a thermomechanical pulp (TMP), a chemico‐TMP (CTMP), and a Kraft mill with a feedstock of primarily black spruce. The primary sludge (PS) and secondary sludge (SS) were mixed at two different ratios (PS:SS = 7:3 and 9:1) and blended with high‐density polyethylene (HDPE) at 20%, 30%, and 40% proportion. The blends were tested using plate–plate geometry before subjection to frequency sweep by oscillation rheometry. The storage modulus (G′), loss modulus (G″), and complex viscosity (η*) increased with increasing paper sludge content. Decreasing the PS:SS ratio from 9:1 to 7:3 decreased G′, G″, and η*. Differential scanning calorimetry showed that sludge addition increased both the melting and crystallization temperature, for a positive effect on crystallinity. Although the behavior of sludge–high‐density polyethylene blends differed from that of traditional wood plastic composite made with wood flour, they obtained G′, G″, and η* values of the same magnitude. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46484.     

Morphology and mechanical properties of biaxially oriented films of polypropylene and HDPE blends

Biaxially oriented films of blends of high-density polyethylene (HDPE) with polypropylene (PP) homopolymer and PP copolymers prepared by twin-screw extrusion and lab-stretcher have been investigated by scanning electron microscopy (SEM), polarized microscopy, differential-scanning calorimeter, and universal testing machine. Three different kinds of PP copolymers were used: (i) ethylene–propylene (EP) random copolymer; (ii) ethylene–propylene (EP) block copolymer; (iii) ethylene–propylene–buttylene (EPB) terpolymer. In the SEM study of the morphology of films of HDPE with various PP blends, phase separation is observed between the PP phase and the HDPE phase for all blends and compositions. In all blends, HDPE serves to reduce the average spherulites size, probably acting as a nucleating agent for PP. The reduction of spherulite size appeared most significantly in the blend of EPB terpolymer and HDPE. A large increase of crystallization temperature was found in the blend of EPB terpolymer and HDPE compared with the unblended EPB terpolymer. For the blend of EPB terpolymer and HDPE, the improvement of tensile strength and modulus is observed with an increase of HDPE content, and this can be considered as a result of the role of HDPE in reducing average spherulite size. © 1994 John Wiley & Sons, Inc.     

Effect of Polyethylene Molecular Architecture on the Dynamic Viscoelastic Behavior of Polyethylene/Polyhexene-1 Blends and Its Correlation with Morphology

In the present work, the rheology, morphology, and interfacial interaction of polyethylene/polyhexane-1 (PE/PH-1) blends with various polyethylene types with different molecular architectures are investigated. The scanning electron microscopy (SEM) images showed a droplet-matrix morphology in all percentage of PH-1 for all blend systems and the size of droplets increased proportionally with PH-1 content. The minimum droplet size is observed for high-density polyethylene (HDPE)/PH-1 blends. The homogeneity of the blends at various compositions is assessed by using viscoelastic parameters determined by dynamic oscillation rheometry in the linear viscoelastic region. A distinct Newtonian plateau at low frequencies is perceived and the variations of complex viscosity (η*) versus angular frequency (ω) for all blend systems are in good agreement with Carreau-Yasuda model. The complex viscosity of samples at various percentages of PH-1 showed the negative deviation from mixing rule in low and high frequencies for all blend systems. The Cole-Cole plots deviated from semi-circular shape at higher percentages of PH-1 than 10wt% in the blends of low-density polyethylene (LDPE)/PH-1 and linear low-density polyethylene (LLDPE)/PH-1. By using emulsion theoretical model, the lowest interfacial tension is found for HDPE/PH-1 blends comparing with its counterparts based on LDPE and LLDPE and the best fitting with experimental data was observed for this blends system.     

Melt miscibility and mechanical properties of metallocene linear low‐density polyethylene blends with high‐density polyethylene: influence of comonomer type

In this paper, the implications of melt miscibility on the thermal and mechanical properties of linear low‐density polyethylene (LLDPE)/high‐density polyethylene (HDPE) blends were assessed with respect to the influence of the comonomer type. The influence of the latter was examined by selecting one butene LLDPE and one octene LLDPE of very similar weight‐average molecular weight (M_w), molecular‐weight distribution (MWD) and branch content, keeping the comonomer type as the only primary molecular variable. Each of the two metallocene LLDPEs was melt‐blended with the same HDPE at 190 °C in a Haake melt‐blender. The rheological, thermal and mechanical properties were measured by the use of an ARES rheometer, differential scanning calorimeter and Instron machine, respectively. The rheological measurements, made over the linear viscoelastic range, suggested no significant influence of the branch type on the melt miscibility. The rheology results are in agreement with those obtained from previous transmission electron microscopy (TEM) and small‐angle neutron scattering (SANS) studies. The dynamic shear viscosity and total crystallinity of the metallocene (m)‐LLDPE blends with HDPE followed linear additivity. At small strains, the branch type has little or no influence on the melt miscibility and solid‐state properties of the blends. Even the large‐strain mechanical properties, such as tensile strength and elongation at break, were not influenced by the comonomer type. However, the ultimate tensile properties of the HDPE‐rich blends were poor. Incompatibility of the HDPE‐rich blends, as a result of the weak interfaces between the blend components, is suggested to develop at large strains. Copyright © 2005 Society of Chemical Industry     

Modification of Ethylene Propylene Diene Terpolymer Rubber by Some Thermoplastic Polymers

Abstract

Blends of ethylene propylene diene terpolymer (EPDM) rubber with thermoplastic polyolefins such as low‐density polyethylene (LDPE), high‐density polyethylene (HDPE), high molecular weight polypropylene (PP), and polypropylene random copolymer grade (PP‐R) were prepared by melt mixing. The physico‐mechanical properties, equilibrium swelling in benzene, and aging properties of the binary blends were investigated, analyzing the effect of the rubber/thermoplastics ratio and the type of the thermoplastic material on these properties. The data obtained indicate that EPDM/PP‐R blend in 20/80 w/w% shows the highest physico‐mechanical properties with improved retained tensile strength at 90°C for 7 days. This blend ratio also gives excellent retained equilibrium swelling in benzene at room temperature for 7 days, although EPDM/LDPE blend in 80/20 w/w% imparts the highest retained elongation at break at 90°C for 7 days.     

Melt rheology of HDPE/EVA blends: The effects of blend ratio,compatibilization, and dynamic vulcanization

The melt rheological behavior of high‐density polyethylene (HDPE)/ethylene vinyl acetate (EVA) blends has been examined with reference to the effect of blend ratio, shear stress, and temperature. The HDPE/EVA blends exhibit pseudoplastic behavior, and the observed rheological behavior of the blends was correlated with the extrudate morphology. The experimental values of the viscosity were compared with the theoretical models. The effect of maleic‐ and phenolic‐modified PE compatibilizers on the viscosity of H₇₀ blend was analyzed and found that compatibilization did not significantly increase the viscosity. The effect of dynamic vulcanization and temperature on the viscosity was also analyzed. The activation energy of the system decreased with increase in EVA content in the system. The phase continuity and phase inversion points of the blends were theoretically predicted and compared with the experimental values. The melt flow index (MFI) values of the blends were also determined and found that the MFI values decreased with increase in EVA content in the system. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers