Crystallization and melting of highly filled polypropylene composites prepared with surface‐treated fillers

Polypropylene (PP) composites with high filler content have been prepared with surface‐treated fillers. The effect of the filler is twofold; nucleation of crystallization occurs, though the PP is also adsorbed onto the filler thereby retarding its motion. Differential scanning calorimetry has been used to study the crystallization of the PP. Melting and recrystallization during melting has been characterized by differential scanning calorimetry. The properties of the composites are more than an additive combination of the filler and polymer. In the case of highly filled composites, the morphology of the PP is important in limiting brittleness and for the strength of the interface between filler and polymer. Surface treatment of the filler has been found to have a significant control over the morphology and properties of the composites. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1942–1948, 2001     

Nonisothermal melt‐crystallization kinetics of syndiotactic polypropylene compounded with various nucleating agents

Nonisothermal melt‐crystallization behavior of syndiotactic polypropylene (sPP) compounded with 5% by weight (wt %) of some inorganic fillers [i.e., kaolin, talcum, marl, titanium dioxide (TiO₂), and silicon dioxide (SiO₂)] and 1 wt % of some organic fillers, which are some sorbital derivatives (i.e., DBS, MDBS, and DMDBS) was investigated and reported for the first time. It was found that the ability of these fillers to nucleate sPP decreased in the following sequence: DBS > talcum > MDBS > SiO₂ ～ kaolin ～ DMDBS > marl > TiO₂, with DBS being able to shift the crystallization exotherm by ～ 18°C on average, while TiO₂ was able to shift the crystallization exotherm by only ～ 6°C on average, from that of neat sPP. The Avrami analysis revealed that the Avrami exponent for sPP compounds varied between 2.9 and 4.3, with the values for neat sPP varying between 3.1 and 6.8. Lastly, the Ziabicki's crystallizability of sPP compounds was greater than that of neat sPP, suggesting an increase in the crystallization ability of sPP as a result of the presence of these fillers. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 245–253, 2005     

Steam‐exploded residual softwood‐filled polypropylene composites

Residual softwood sawdust was pretreated by a steam‐explosion technique. It was used as a natural filler in polypropylene (PP)‐based composites. Dynamic mechanical analysis and tensile properties of these materials were studied. The influence of filler loading, steam‐explosion severity, and coating the fiber with a functionalized compatibilizer, such as maleic anhydryde polypropylene (MAPP), on the mechanical behavior of the composite was evaluated. The results were analyzed in relation with scanning electron microscopy observations, and surface energy (dispersive and polar components) and apparent specific area measurements. Experimental data indicate a better compatibility between MAPP‐coated fiber and PP with respect to the untreated one. The coating treatment of the softwood fiber was found to promote interfacial adhesion between both components, and to enhance the tensile properties of the resulting composite. This reinforcing effect was well predicted from theoretical calculations based on a mean field approach (Halpin‐Kardos model). The steam‐explosion pretreatment severity increased the surface energy and apparent specific surface, and resulted in a loss of the fiber entirety. The sorption behavior of these composite materials was also performed. It was found that the composites absorb more water, as the filler content is higher. MAPP coating provided protection from water uptake in the interphase region. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 74: 1962–1977, 1999     

Isothermal crystallization kinetics of polypropylene in melt‐mixed composites of polypropylene and multi‐walled carbon nanotubes

The isothermal crystallization behaviour of the polypropylene (PP) phase in PP/multi‐walled carbon nanotubes (MWCNTs) composites has been investigated via differential scanning calorimetric analysis, which showed the influence of the varying dispersion level of MWCNTs in the respective PP matrix. PP/MWCNTs composites were prepared via melt‐blending technique, wherein two different grades of MWCNTs of varying average “agglomerate” size and varying entanglements (N‐MWCNTs and D‐MWCNTs) were utilized. Furthermore, the influence of melt‐viscosity of the PP phase was investigated on the crystallization kinetics of the PP/MWCNTs composites. Heterogeneous nucleation ability of MWCNTs has resulted in a decrease in half time of crystallization (t _1/2) from ～14 min for pure PP to ～6 min for PP/N‐MWCNTs and ～11 min for PP/D‐MWCNTs composites at 1 wt% of MWCNTs at 132 °C. Overall rate of crystallization (k) has significantly increased to 4.9 × 10^?2 min^?1 for PP/N‐MWCNTs composite as compared with 6.2 × 10^?3 min^?1 for PP/D‐MWCNTs composite at 0.5 wt% of MWCNTs at 132 °C. Moreover, the effect of a novel organic modifier, Li‐salt of 6‐amino hexanoic acid along with a compatibilizer (PP‐g‐MA) has also been investigated on the crystallization kinetics of the PP phase in PP/MWCNTs composites. POLYM. ENG. SCI., 57:1136–1146, 2017. © 2017 Society of Plastics Engineers     

Keratin–polyhydroxyalkanoate melt‐compounded composites with improved barrier properties of interest in food packaging applications

Sustainable biocomposite materials based on the combination of polyhydroxyalkanoates with a keratin additive derived from poultry feathers were successfully developed via melt compounding. Suitable dispersions for low loadings of the additive in the biopolymeric matrix were achieved by the melt‐mixing technique. A good physical interaction between the polymeric matrix and the additive was observed by scanning electron microscopy (SEM). Reductions in water, limonene, and oxygen permeability of the pure polymer to less than a half of its initial value for the composite containing 1 wt % of keratin additive were achieved. This composition was also found to exhibit optimum mechanical performance. As a result, these materials offer significant potential in fully renewable packaging applications based on polyhydroxyalkanoates with enhanced barrier performance. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39947.     

Crystallization behavior of carbon black‐filled polypropylene and polypropylene/epoxy composites

The crystallization behavior of polypropylene (PP)/carbon black (CB) and PP/epoxy/CB composites was studied with differential scanning calorimetry (DSC). The effects of compatibilizer MAH‐g‐PP and dynamic cure on the crystallization behavior are investigated. The nonisothermal crystallization parameters analysis showed that CB particles in the PP/CB composites and the dispersed epoxy particles in the PP/epoxy composites could act as nucleating agents, accelerating the crystallization of the composites. Morphological studies indicated that the incorporation of CB into PP/epoxy resulted in its preferential localization in the epoxy resin phase, changing the spherical epoxy particles into elongated structure, and thus reduced the nucleation effect of epoxy particles. Addition of MAH‐g‐PP significantly decreased the average diameter of epoxy particles in the PP/epoxy and PP/epoxy/CB composites, promoting the crystallization of PP more effectively. The isothermal crystallization kinetics and thermodynamics of the PP/CB and PP/epoxy/CB composites were studied with the Avrami equation and Hoffman theory, respectively. The Avrami exponent and the crystallization rate of the PP/CB composites were higher than those of PP, and the free energy of chain folding for PP crystallization decreased with increasing CB content. Addition of MAH‐g‐PP into the PP/epoxy and PP/epoxy/CB composites increased the crystallization rate of the composites and decreased the chain folding energy significantly. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 104–118, 2006     

Structure development in thermoset recyclate‐filled polypropylene composites

Polypropylene containing comminuted fiber reinforced thermoset recyclate has been shown to exhibit enhanced mechanical properties relative to particulate‐filled materials. Optimum mechanical performance in these recyclate‐filled materials is achieved in compositions made from rubber‐modified polypropylene containing maleic anhydride‐modified PP in conjuction with silane coupling agent. Although matrix crosslinking was found to enhance properties in both filled and unfilled systems, composite properties are dominated by the development of strong interfacial bonding between polypropylene and recyclate reinforcement. A mechanism for the formation of interfacial bonding is proposed involving reaction between maleic anhydride functionalized PP, formation of trisilanol groups and their subsequent condensation with hydroxyl groups on the recyclate surfaces, together with molecular entanglement and co‐crystallization of the grafted and ungrafted polypropylene molecules. Furthermore, in the absence of treatment there is evidence that the elastomer particles encapsulate the filler particles. However, this effect is strongly hindered when functionalized‐PP is added, either in isolation or in combination with the silane co‐treatment. The crystalline nucleation of PP by thermoset recyclate and treatment is also considered. The treatment system investigated was found to promote interfacial bonding to both the polyester (DMC) and woven glassreinforced phenolic recyclates investigated, suggesting it may be suitable for treating mixed composite scrap.     

Tensile properties of hollow glass bead‐filled polypropylene composites

The tensile properties of polypropylene (PP) filled with hollow glass beads have been measured at room temperature to identify the effects of the particle contents, size and its distribution on them in the present article. The mean diameters of the fillers were 11, 35, and 70 μm, and they were named as TK10, TK35, and TK70 respectively. The surface of these particles was pretreated with silane coupling agent. The results showed that the yield stress (σ_y) decreased gently for PP/TK70 systems, whereas decreased relatively obviously for PP/TK35 systems with increasing the volume fraction (?_f) of the fillers. When ?_f was less than 5%, the tensile strength at break (σ_b) of the composites increased with the increase of ?_f. When ?_f was more than 5%, σ_b was almost a constant for PP/TK70 systems, while σ_b decreased linearly for PP/TK35 systems. The tensile fracture strain (ε_b) of the composites decreased suddenly when ?_f was less than 5%, and then decreased slightly with increasing ?_f. When ?_f was 10%, σ_y and σ_b increased while ε_b decreased with the increase of the bead diameter. Furthermore, the σ_y was predicted by means an equation proposed in the previous work, and good interfacial adhesion was shown between the hollow glass beads and the matrix. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 1697–1701, 2007     

Flammability and mechanical properties of wood flour‐filled polypropylene composites

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

Impact fracture toughness and morphology of diatomite‐filled polypropylene composites

Impact fracture strength is an important characterization for impact toughness of materials. A polypropylene (PP) filled with diatomite with different diameter (5, 7, and 13 μm) was fabricated by means a twin‐screw extruder. The impact fracture strength of these composites was measured at room temperature to identify the effects of diatomite content and diameter on impact fracture strength of filled polypropylene composites. The results showed that the influence of diatomite on the notched impact strength was significant. When the volume fraction of the diatomite (?_f) was less than 10%, the notched impact strength (σ_I) increased quickly with an addition of ?_f, and then the variation of σ_I was slight. The notched impact strength of the composite with the diatomite diameter of 7 μm is the highest when ?_f was 10%. Furthermore, the impact fracture surface was observed by using a scanning electronic microscope (SEM) to study the toughening mechanisms. POLYM. ENG. SCI., 2009. © 2009 Society of Plastics Engineers     

Water absorption and dimensional stability of short kenaf fiber‐filled polypropylene composites treated with maleated polypropylene

The purpose of this research was to investigate the water absorption behavior and associated dimensional stability of kenaf‐polypropylene‐filled (PP/KF) composites. Composites with different fiber loadings, ranging from 0 to 40 wt %, were prepared with a twin‐screw extruder followed by hot press molding. The influence of the compatibilizer was also studied for PP/KF composite with 5 wt % maleated PP (MAPP). Water absorption testing was carried out at room temperature for 7 weeks. Tensile, flexural, and impact tests were also performed on control, wet, and re‐dried specimens. Increasing the fiber content resulted in higher water absorption and thickness swelling. The inferior mechanical properties of the wet composites were attributed to the effect of water, which deteriorates the interfacial properties of composites. On re‐drying, all properties were almost recovered because of the recovery of interfacial area as evident in scanning electron micrographs. Incorporation of the MAPP significantly improved the compatibility between the fiber and matrix and the mechanical properties of the composites compared with those without MAPP. It also diminished the water absorption as well as the related thickness swelling in the composites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Nonisothermal melt‐crystallization kinetics of hydroxyapatite‐filled poly(3‐hydroxybutyrate) composites

The knowledge of biomedical implants ranging from drug delivery devices to tissue engineering and based on bioresorbable polymer composites is increasing, but the study of the crystallization kinetics of these kinds of composites is seldom a concern. The focus of our experimental research was the nonisothermal‐crystallization behavior of poly(3‐hydroxybutyrate) (PHB)/hydroxyapatite (HA) composites, which was monitored by means of differential scanning calorimetry at different cooling rates. Various macrokinetic models were applied to describe the process of nonisothermal crystallization. The results showed that the modified Avrami model and Mo's approach could describe the nonisothermal crystallization of the composites very well, but the Ozawa analysis alone was thought to be rather inapplicable. The values of the half‐time and kinetic crystallizability showed that the crystallization rate increased with increasing cooling rates for both PHB and the composites. The HA particles served as additional nucleation sites, and low levels of HA resulted in dramatic increases in the crystallization rate with respect to pure PHB; however, high HA contents (> 20 wt %) clearly retarded the growth process. The activation energy for nonisothermal crystallization was evaluated with the Kissinger method and was found to vary with the incorporation of HA. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:5388–5395, 2006     

Influence of grafted polypropylene on the mechanical properties of mineral‐filled polypropylene composites

The purpose of this work was to study how mineral fillers would behave in a polypropylene (PP) matrix when PP modified with maleic anhydride (MA) and/or itaconic acid (IA) was used as a coupling agent in the preparation of mineral‐filled PP composites. The composites were characterized with tensile mechanical measurements and morphological analysis. The optimum amount of the coupling agent to be used to obtain composites with improved mechanical properties was established. The results indicated that these coupling agents enhanced the tensile strength of the composites significantly, and the extent of the coupling effect depended on the nature of the interface that formed. The incorporation of coupling agents enhanced the resistance to deformation of the composite. The behavior of IA‐modified PP as a coupling agent was similar to that of a commercial MA‐modified PP for the filled PP composites. Evidence of improved interfacial bonding was revealed by scanning electron microscopy studies, which examined the surfaces of fractured tensile test specimens; their microstructures confirmed the mechanical results with respect to the observed homogeneous or optimized dispersion of the mineral‐filler phase in these composites. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2343–2350, 2007     

Rheological behaviors of glass bead‐ and wollastonite‐filled polypropylene composites modified with thermoplastic elastomers

Steady‐ and oscillatory‐shear rheological behaviors of polypropylene/glass bead (PP/GB) and PP/wollastonite (PP/W) melts modified with thermoplastic elastomers, poly(styrene‐b‐ethylene‐co‐butylene‐b‐styrene) copolymer (SEBS) and the corresponding block copolymer grafted with maleic anhydride (SEBS‐g‐MA), were examined by means of a parallel‐plate rheometer. With adding the elastomers (SEBS and SEBS‐g‐MA) and fillers (spherical GB and acicular W) to PP, viscosity especially at low shear rates and shear‐thinning flow behavior at high shear rates were pronounced as evidenced quantitatively by Carreau–Yasuda (CY) parameters, but Cox–Merz analogy became weakened. Besides, melt‐elasticity in terminal region and relaxation time (t_c) in crossing point increased, indicating an enhancement in quasi‐solid behavior of molten PP. Comparing with the elastomers, rheological behaviors of molten PP were more influenced with adding the rigid fillers, especially with W due to distinct acicular shape of W particles. SEBS‐g‐MA elastomer more affected rheological behaviors of the ternary composites than SEBS elastomer, implying that SEBS elastomer and the filler particles behaved individually (i.e., development of separate microstructure) in (PP/GB)/SEBS and (PP/W)/SEBS ternary composites, but core‐shell microstructure developed with strong interfacial adhesion by adding SEBS‐g‐MA elastomer, and the filler particles encapsulated with the thick SEBS‐g‐MA elastomer interlayer (i.e., core‐shell particles) acted like neither big elastomer particles nor like individual rigid particles in melt‐state. Moreover, effects of SEBS‐g‐MA elastomer reached a maximum on rheological behaviors of (PP/W)/SEBS‐g‐MA ternary composite, indicating a synergy between core‐shell microstructure and acicular W particles. Correlations between oscillatory‐shear flow properties and microstructures of the blends and composites were evaluated using Cole–Cole (CC), Han–Chuang (HC), and van Gurp–Palmen (vGP) plots. COMPOS., 2012. © 2012 Society of Plastics     

Evaluation of dynamic elastic properties of wood‐filled polypropylene composites

Dynamic modulus of elasticity (MoE) and shear modulus of wood‐filled polypropylene composite at various filler contents ranging from 10% to 50% was determined from the vibration frequencies of disc‐shaped specimens. Wood filler was used in both fiber form (pulp) and powder form (wood flour). A novel compatibilizer, m‐isopropenyl‐α,α‐dimethylbenzyl‐isocyanate(m‐TMI) grafted polypropylene with isocyanate functional group was used to prepare the composites. A linear increase in dynamic MoE, shear modulus, and density of the composite was observed with the increasing filler content. Between the two fillers, wood fiber filled composites exhibited slightly better properties. At 50% filler loading, dynamic MoE of the wood fiber filled composite was 97% higher than that of unfilled polypropylene. Halpin‐Tsai model equation was used to describe the changes in the composite modulus with the increasing filler content. The continuous improvement in elastic properties of the composites with the increasing wood filler is attributed to the effective reinforcement of low‐modulus polypropylene matrix with the high‐modulus wood filler. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 1706–1711, 2006     

Mechanical properties of glass bead‐ and wollastonite‐filled isotactic‐polypropylene composites modified with thermoplastic elastomers

Mechanical properties of the isotactic‐polypropylene/glass bead (iPP/GB) and iPP/wollastonite (iPP/W) composites modified with thermoplastic elastomers, the poly(styrene‐b‐ethylene‐co‐butylene‐b‐styrene) copolymer (SEBS) and corresponding block copolymer grafted with maleic anhydride (SEBS‐g‐MA), were investigated. An increase in toughness of iPP with the elastomers was associated with a decrease in rigidity and strength. Mechanical performance of iPP increased more with acicular W than with spherical GB due to reinforcing effect of W. Comparing the (iPP/GB)/SEBS and (iPP/W)/SEBS composites having the separate microstructure, strength and toughness values of the iPP/GB and iPP/W composites increased more with SEBS‐g‐MA at the expense of rigidity due to the core‐shell microstructure with strong interfacial adhesion. Moreover, the iPP/W composite exhibited superior mechanical performance with 2.5 and 5 vol% of SEBS‐g‐MA because of a positive synergy between the core‐shell microstructure and reinforcing effect of acicular W. The extended models revealed that the elastomer and filler particles in the (iPP/GB)/SEBS and (iPP/W)/SEBS composites acted individually due to the separate microstructure. However, the rigid GB and W particles encapsulated with the thick elastomer interlayer (R₀/R₁ = 0.91) in the (iPP/GB)/SEBS‐g‐MA and (iPP/W)/SEBS‐g‐MA composites acted like neither big elastomer particles nor like individual rigid particles, inferring more complicated failure mechanisms in the core‐shell composites. POLYM. COMPOS., 31:1285–1308, 2010. © 2010 Society of Plastics Engineers     

Microstructural characteristics of glass bead‐ and wollastonite‐filled isotactic‐polypropylene composites modified with thermoplastic elastomers

Microstructural characteristics of isotactic‐polypropylene/glass bead (iPP/GB) and iPP/wollastonite (iPP/W) composites modified with thermoplastic elastomers, poly(styrene‐b‐ethylene‐co‐butylene‐b‐styrene) copolymer (SEBS) and corresponding block copolymer grafted with maleic anhydride (SEBS‐g‐MA), were investigated. Scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and dynamic mechanical analyses (DMA) showed that the iPP/SEBS and iPP/SEBS‐g‐MA blends were partially compatible two‐phase systems. Well‐dispersed spherical GB and acicular W particles without evidence of interfacial adhesion were observed in the iPP/GB and iPP/W binary composites respectively. Contrary to the blends, melt flow rates of the iPP/GB and PP/W composites decreased more with SEBS‐g‐MA than with SEBS because of enhanced interfacial adhesion with SEBS‐g‐MA elastomer. The SEM analyses showed that the ternary composites containing SEBS exhibited separate dispersion of the rigid filler and elastomer particles (i.e., separate microstructure). However, SEBS‐g‐MA elastomer not only encapsulated the spherical GB and acicular W particles completely with strong interfacial adhesion (i.e., core‐shell microstructure) but also dispersed separately throughout iPP matrix. In accordance with the SEM observations, the DSC and DMA revealed quantitatively that the rigid filler and SEBS particles in iPP matrix acted individually, whereas the rigid filler particles in the ternary composites containing SEBS‐g‐MA acted like elastomer particles because of the thick elastomer interlayer around the filler particles. The Fourier transform infrared analyses revealed an esterification reaction inducing the strong interfacial adhesion between the SEBS‐g‐MA phase and the filler particles. POLYM. COMPOS., 31:1265–1284, 2010. © 2009 Society of Plastics Engineers     

Ink‐eliminated waste paper sludge flour‐filled polypropylene composites with different coupling agent treatments

Ink‐eliminated sludge flour (IESF), waste residue from the recycling treatments of waste paper, was utilized as a new kind of filler to reinforce polypropylene (PP) in this research work. Different coupling agents, including maleated anhydride grafted PP (MAPP), stearic acid (SA), and titanate (NDZ‐101), were used to increase the compatibility between IESF and PP. By using different measurements, the microstructure, morphology, thermal behaviors, and mechanical properties of the IESF/PP composites were investigated in detail. It was found that IESF, as a nucleation agent, not only induced the crystallization orientation of PP but also accelerate the crystallization rate of PP. Just as indicated in the experiments, the presence of IESF has shown the advantages of increasing the dimensional stability, the hardness and the flexural property, and the presence of coupling agents has a favorable effect on the improvement of dimensional stability. Moreover, the coupling agent has minor influence on the mechanical property, even causes some decrease in the impact strength. Among these three coupling agents, MAPP is found to be the best coupling agent for increasing the interfacial adhesion between IESF and PP, and the MAPP addition makes the PP composite possess the quickest crystallization rate and greatest tensile strength. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 513–520, 2003     

Rheological behavior of coir‐fiber‐filled polypropylene composites at constant shear stress

The rheological behavior of coir‐fiber‐filled polypropylene (PP) composite has been studied at constant shear stress. The shear stress versus shear rate relationship for the composite follows power law model of viscous flow. Unlike similar studies in the literature, the viscosity is treated as a stress‐independent parameter, which increases with the increase of fiber loading; but decreases with the rise of temperature. The SEM reveals that the fibers are loosely bound to the polymer matrix and the outer surface of the composite is rough and irregular, making it susceptible to high friction with the wall of the flow channel. With analogy to nth order chemical reaction, new formula has been derived for the activation energy of viscous flow, which is found to increase with the increase in the fiber content. The die‐swell ratio decreases with the increase of fiber loading, but increases with the rise of temperature. The elastics parameters of the composite such as the recoverable shear strain, the first normal stress difference, and the elastic strain induced by the stored energy in the capillary reservoir have been estimated based on the die‐swell data. POLYM. COMPOS., 36:51–61, 2015. © 2014 Society of Plastics Engineers