Effects of a new compatibilizer system on the flexural properties of wood–polyethylene composites

A novel wood–plastic compatibilizer system containing a paper wet‐strength agent as a wood‐binding domain and stearic anhydride as a polyethylene (PE) binding domain was investigated. Treatment of wood flour with a commercial paper wet‐strength agent Kymene® 557H (simply called Kymene) before the mixing of PE and the wood flour increased the modulus of rupture (MOR) and the modulus of elasticity (MOE) of the resulting wood–PE composites. Addition of stearic acid in the mixing of PE and the wood–Kymene mixture further increased the MOR and MOE. Stearic anhydride was even more effective than stearic acid in the increase of the MOR and MOE. Compared to wood–PE composites without a compatibilizer, the stearic anhydride–Kymene compatibilizer system increased the MOR by about 33% and the MOE by about 40%. The stearic anhydride–Kymene compatibilizer system gave a slightly lower MOR, but higher MOE than those of the commercially used compatibilizer (maleic anhydride‐grafted polypropylene). The compatibilization mechanisms were proposed as follows: Kymene not only bound to wood fibers, but also strengthened and stiffened the wood fibers. Stearic anhydride formed covalent linkages such as ester and amide with the Kymene‐consolidated wood fibers and the long hydrocarbon chain of the stearic anhydride bonded to the PE matrix through entanglements and/or cocrystallization. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 3667–3672, 2004     

Foam extrusion of high density polyethylene/wood‐flour composites using chemical foaming agents

A one‐way analysis of variance and thermal analysis were performed in this study to examine the influences of the contents, types (exothermic vs. endothermic), and forms (pure vs. masterbatch) of chemical foaming agents (CFAs), as well as the use of coupling agents, on the density reduction (or void fraction) and cell morphology of extrusion‐foamed neat high density polyethylene (HDPE) and HDPE/wood‐flour composites. The CFA types and forms did not affect the void fractions of both the neat HDPE and HDPE/wood‐flour composites. However, a gas containment limit was observed for neat HDPE foams whereas the average cell size achieved in the HDPE/wood‐flour composite foams remained insensitive to the CFA contents, irrespective of the foaming agent types. The experimental results indicated that the use of coupling agent in the formulation was required to achieve HDPE/wood‐flour composite foams with high void fraction. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 3139–3150, 2003     

Surface chemistry and mechanical property changes of wood‐flour/high‐density‐polyethylene composites after accelerated weathering

Although wood–plastic composites have become more accepted and used in recent years and are promoted as low‐maintenance, high‐durability building products, they do experience a color change and a loss in mechanical properties with accelerated weathering. In this study, we attempted to characterize the modulus‐of‐elasticity (MOE) loss of photostabilized high‐density polyethylene (HDPE) and composites of wood flour and high‐density polyethylene (WF/HDPE) with accelerated weathering. We then examined how weathering changed the surface chemistry of the composites and looked at whether or not the surface changes were related to the MOE loss. By examining surface chemistry changes, we hoped to begin to understand what caused the weathering changes. The materials were left unstabilized or were stabilized with either an ultraviolet absorber or pigment. After 1000 and 2000 h of accelerated weathering, the samples were tested for MOE loss. Fourier transform infrared (FTIR) spectroscopy was employed to monitor carbonyl and vinyl group formation at the surface. Changes in the HDPE crystallinity were also determined with FTIR techniques. It was determined that structural changes in the samples (carbonyl group formation, terminal vinyl group formation, and crystallinity changes) could not be reliably used to predict changes in MOE with a simple linear relationship. This indicated that the effects of crosslinking, chain scission, and crystallinity changes due to ultraviolet exposure and interfacial degradation due to moisture exposure were interrelated factors for the weathering of HDPE and WF/HDPE composites. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 2263–2273, 2004     

The effect of zinc oxide addition on the compatibilization efficiency of maleic anhydride grafted high‐density polyethylene compatibilizer for high‐density polyethylene/polyamide 6 blends

A high‐density polyethylene with grafted maleic anhydride units has been investigated as a compatibilizer for high‐density polyethylene with polyamide 6. The material acts as an effective compatibilizer, causing a marked reduction in dispersed phase size as well as an increase in tensile strength and toughness. Compatibilizer also affects the glass‐transition temperature, crystallization kinetics, and amount of crystalline material for certain blend compositions. The addition of zinc cations, which are effective in increasing ethylene‐acid copolymer compatibilizer performance in low‐density polyethylene/polyamide blends, has little, if any, effect on compatibilizer performance in these high‐density polyethylene/polyamide blends. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3871–3881, 2007     

In‐process ultrasonic measurements of orientation and disorientation relaxation of high‐density polyethylene/polyamide‐6 composites with compatibilizer

The relaxation processes of orientation and disorientation of melts of high‐density polyethylene (HDPE) and polyamide‐6 (PA6) blends compatibilized with a compatibilizer precursor (CP) of HDPE‐grafted maleic anhydride (HDPE‐g‐MAH) were investigated in a restricted channel using real‐time ultrasonic technique. The experimental results showed that the evolution of ultrasonic velocity of HDPE/PA6 blends during the orientation or disorientation processes could be described by the exponential equation from which the maximum orientation degree and relaxation time could be obtained. Subsequently, the effects of CP on the relaxation processes of orientation and disorientation were studied. In addition, the relations of the CP content and the morphology and viscosity were investigated by scanning electron microscope analysis and rheological tests. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Wood‐thermoplastic composites from wood flour and high‐density polyethylene

High‐density polyethylene/wood flour (HDPE/WF) composites were prepared by a twin‐screw extruder. The effects of WF, silane coupling agents, polymer compatibilizers, and their content on the comprehensive properties of the WF/HDPE composites have been studied in detail, including the mechanical, thermal, and rheological properties and microstructure. The results showed that both silane coupling agents and polymer compatibilizers could improve the interfacial adhesion between WF and HDPE, and further improve the properties of WF/HDPE composites, especially with AX8900 as a compatibilizer giving higher impact strength, and with HDPE‐g‐MAH as a compatibilizer giving the best tensile and flexural properties. The resultant composite has higher strength (tensile strength = 51.03 MPa) and better heat deflection temperature (63.1°C). © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of fiber length on processing and properties of extruded wood‐fiber/HDPE composites

Fiber length and distribution play important roles in the processing and mechanical performance of fiber‐based products such as paper and fiberboard. In the case of wood–plastic composites (WPC), the production of WPC with long fibers has been neglected, because they are difficult to handle with current production equipment. This study provides a better understanding of the effect of fiber length on WPC processing and properties. The objectives of this study were therefore to determine the role of fiber length in the formation process and property development of WPC. Three chemithermomechanical pulps (CTMP) with different lengths, distributions, and length‐to‐diameter ratios (L/D) were obtained by mechanical refining. Length, shape, and distribution were characterized using a fiber quality analyzer (FQA). The rheometer torque properties of high‐density polyethylene (HDPE) filled with the pulps at different loads were studied. Variations in fiber load and length distribution resulted in significant variations in melting properties and torque characteristics. Composites from the three length distributions were successfully processed using extrusion. Physical and mechanical properties of the obtained composites varied with both length distribution and additive type. Mechanical properties increased with increasing fiber length, whereas performance in water immersion tests decreased. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Ultraviolet weathering of photostabilized wood‐flour‐filled high‐density polyethylene composites

Wood‐plastic composites are being increasingly examined for nonstructural or semistructural building applications. As outdoor applications become more widespread, durability becomes an issue. Ultraviolet exposure can lead to photodegradation, which results in a change in appearance and/or mechanical properties. Photodegradation can be slowed through the addition of photostabilizers. In this study, we examined the performance of wood flour/high‐density polyethylene composites after accelerated weathering. Two 2⁴ factorial experimental designs were used to determine the effects of two hindered amine light stabilizers, an ultraviolet absorber, a colorant, and their interactions on the photostabilization of high‐density polyethyl‐ ene blends and wood flour/high‐density polyethylene composites. Color change and flexural properties were determined after 250, 500, 1000, and 2000 h of accelerated weathering. The results indicate that both the colorant and ultraviolet absorber were more effective photostabilizers for wood flour/high‐density polyethylene composites than the hindered amine light stabilizers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2609–2617, 2003     

Effect of polyethylene‐graft‐maleic anhydride as a compatibilizer on the mechanical and tribological behaviors of ultrahigh‐molecular‐weight polyethylene/copper composites

Ultrahigh‐molecular‐weight polyethylene/copper (UHMWPE/Cu) composites compatibilized with polyethylene‐graft‐maleic anhydride (PE‐g‐MAH) were prepared by compression molding. The effects of the compatibilizer on the mechanical, thermal, and tribological properties of the UHMWPE/Cu composites were investigated. These properties of the composites were evaluated at various compositions, and worn steel surfaces and composite surfaces were examined with scanning electron microscopy and X‐ray photoelectron spectroscopy. The incorporation of PE‐g‐MAH reduced the melting points of the composites and increased their crystallinity to some extent. Moreover, the inclusion of the PE‐g‐MAH compatibilizer greatly increased the tensile rupture strength and tensile modulus of the composites, and this improved the wear resistance of the composites. These improvements in the mechanical and tribological behavior of the ultrahigh‐molecular‐weight‐polyethylene‐matrix composites with the PE‐g‐MAH compatibilizer could be closely related to the enhanced crosslinking function of the composites in the presence of the compatibilizer. Moreover, the compatibilizer had an effect on the transfer and oxidation behavior of the filler Cu particulates, which could be critical to the application of metallic‐particulate‐filled polymer composites in engineering. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 948–955, 2004     

Comparative study of maleated polyolefins as compatibilizers for polyethylene/wood flour composites

The effects of various types of compatibilizers on the mechanical properties of high‐density polyethylene/wood flour composites were investigated. Functionalized polyolefins, including maleated polyethylenes, polypropylene, and styrene–ethylene/butylene–styrene copolymer, were incorporated to reduce the interfacial tension between the polyethylene matrix and wood filler. Of these, maleated linear low‐density and high‐density polyethylenes gave higher tensile and impact strengths for the composites, presumably because of their better compatibility with the high‐density polyethylene matrix. Similar but less enhanced improvements in the mechanical properties, depending on the compatibilizer loading, were seen for a maleated styrene–ethylene/butylene–styrene triblock copolymer, whereas maleated polypropylene only slightly improved the tensile modulus and tensile strength, which increased with increasing compatibilizer loadings. Scanning electron microscopy was used to reveal the interfacial region and confirm these findings. Dynamic mechanical thermal measurements showed the interaction between the filler and the matrix. Fourier transform infrared spectroscopy was used to assign the chemical fixation and the various chemical species involved on the surfaces of the fillers before and after surface treatment. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 87: 487–496, 2003     

Creep resistance of wood‐filled polystyrene/high‐density polyethylene blends

Creep, the deformation over time of a material under stress, is one characteristic of wood‐filled polymer composites that has resulted in poor performance in certain applications. This project was undertaken to investigate the advantages of blending a plastic of lower‐creep polystyrene (PS) with high‐density polyethylene (HDPE) at ratios of 100:0, 75:25, 50:50, 25:75, and 0:100. These various PS–HDPE blends were then melt blended with a short fiber‐length wood flour (WF). Extruded bars of each blend were examined to measure modulus of elasticity and ultimate stress. Increasing the ratio of WF increased modulus of elasticity in all composites, except between 30 and 40% WF, whereas the effect of WF on ultimate stress was variable, depending on the composite. Scanning electron microscopic images and thermal analysis indicated that the wood particles interacted with the PS phase, although the interactions were weak. Finally, creep speed was calculated by using a three‐point bending geometry with a load of 50% of the ultimate stress. Creep decreased only slightly with increasing WF content but more significantly with increasing PS content, except at pure PS. The WF/75PS–25HDPE blend showed the least creep. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 418–425, 2001     

Influence of mineral fillers on the fire retardant properties of wood‐polypropylene composites

The effects of mineral fillers on the fire retardancy of wood‐polypropylene composites have been studied. Wood‐polypropylene composites containing mineral fillers have been compounded in a conical twin‐screw extruder. A composite manufactured without any mineral filler addition has been used as a reference. The flame resistance properties of the composite materials have been studied using the cone calorimeter. The results show that the introduction of mineral fillers into the wood‐polypropylene composites has a favourable effect on the fire resistance properties of the composite materials. The reaction‐to‐fire properties have been improved according to the fire classification of construction products based on the Euroclass system. Copyright © 2012 John Wiley & Sons, Ltd.     

Surface characterization of weathered and heat‐treated wood‐based composites reinforced by styrene maleic anhydride

The aim of this study was to investigate the effect of heat‐treated lignocellulosic filler on the surface characteristics and decay resistance of the wood flour/styrene maleic anhydride (SMA) composites. In this study, heat treatment was conducted at 212°C for 8 hours. Test specimens were prepared by injection molding at 220°C. Weathering tests were performed by cycles of UV‐light irradiation for 8 hours, water spray for 15 minutes, and then conditioning for 3.45 hours in an accelerated weathering test cycle chamber. Heat‐treated wood flour/SMA composites were evaluated for color changes, and attenuated total reflectance Fourier transform infrared (FTIR) spectroscopy was used to analyze chemical changes on the sample surfaces. The wood decay tests were performed of white rot fungus, Trametes versicolor (L.: Fr.) Pilat was based on mini‐block specimens on 48% malt extract agar in petri dishes. The study showed that color changes occurred when heat‐treated filler rate is increased in this material. Therefore, materials in 10% filler rate show lower color changes than other variation. As a result of the FTIR analysis, the addition of wood filler into the SMA causes changes in the chemical structure. In addition, the increase in wood filler reduced the resistance to weathering. Decay results showed that thermally modified wood has lower mass loss caused by fungal attack than untreated wood material. The weight loss decreases with the increase in wood flour rate expect 10%T and 10%UT in all composites.     

Photoaging and stabilization of rigid PVC/wood‐fiber composites

Ultraviolet (UV) weathering performance of unpigmented and rutile titanium dioxide pigmented rigid polyvinyl chloride (PVC)/wood‐fiber composites has been studied. The composite samples were manufactured by dry‐blending PVC, wood fibers, and other processing additives in a high‐intensity mixer. The dry‐blended compounds were extruded and compression molded into panel samples. The manufactured samples were artificially weathered using laboratory accelerated UV tests. Composite samples were exposed to 340‐nm fluorescent UV lamps and assessed every 200 h, for a total of 1200 h of accelerated weathering. Each assessment consisted of a visual examination of surface roughness or erosion, a contact angle measurement, a FTIR collection, and a color measurement. The experimental results indicated that wood fibers are effective sensitizers and that their incorporation into a rigid PVC matrix has a deleterious effect on the ability of the matrix to resist degradation caused ultraviolet irradiation. The light stability of these composites could be improved quite efficiently with the addition of rutile titanium dioxide photoactive pigment during formulation. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1943–1950, 2001     

Synthesis of polypropylene‐graft‐maleic anhydride compatibilizer and evaluation of nylon 6/polypropylene blend properties

Polymer blends based on polyolefins are of a great interest owing to their broad spectrum of properties and practical applications. However, because of poor compatibilities of components, most of these systems generally exhibit high interfacial tension, a low degree of dispersion and poor mechanical properties. It is generally accepted that polypropylene (PP) and nylon 6 (N6) are not compatible and that their blending results in poor materials. The compatibility can be improved by the addition of a compatibilizer, and in this study PP was functionalized by maleic anhydride (MAH) in the presence of an optimized amount of dicumyl peroxide (DCP). The reaction was carried out in the molten state using an internal mixer. Then, once the compatibilizer polypropylene‐graft‐maleic anhydride (PP‐g‐MAH) was prepared, it was added at various concentrations (2.5–10 wt%) to 30/70 glass fibre reinforced N6 (GFRN6) PP, and the mechanical properties were evaluated. It was found that the incorporation of the compatibilizer enhanced the tensile properties (tensile strength and modulus) as well as the Izod impact properties of the notched samples. This was attributed to better interfacial adhesion as evidenced by scanning electron microscopy (SEM). The optimum in these properties was achieved at a critical PP‐g‐MAH concentration. Copyright © 2005 Society of Chemical Industry     

Mechanical properties of wood flake–polyethylene composites. II. Interface modification

This article discusses the methods of interface modification of composites based on raw wood flakes and high‐density polyethylene (HDPE) and the effects of these modifications on composite properties. An HDPE matrix was modified by a reaction with maleic anhydride (MA) in a twin‐screw extruder and then compounded with wood flakes to produce wood–polyethylene composites. Wood flakes were modified by a reaction with a silane coupling agent in an aqueous medium before being compounded with HDPE to produce silane‐modified WPCs. Differential scanning calorimetry and Fourier transform infrared spectroscopy data provide evidence for the existence of a polyethylene (PE)–silane‐grafted wood structure, which acts as a compatibilizer for wood flakes and PE. The results of MA‐modified composites indicate that some maleated HDPE is reacting with wood through esterification to form a compatibilizer for wood flakes and HDPE. Significant improvements in tensile strength, ductility, and Izod impact strength were obtained. Scanning electron micrographs provide evidence for strong interactions between the wood flakes and the matrix agent. The results indicate that 1–2 wt % MA modification on HDPE and 1–3 wt % silane treatment on wood flakes provide WPCs with the optimum properties. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2505–2521, 2002     

Effect of epoxy functionalized compatibilizer on the mechanical properties of low‐density polyethylene/plasticized tapioca starch blends

A series of low‐density polyethylene (LDPE) blends with varying proportions of plasticized tapioca starch have been used for the study of their mechanical properties. A functionalized epoxy resin, namely, poly(ethylene‐co‐glycidyl methacrylate) has been used as the compatibilizer. The impact and tensile properties have been measured by standard ASTM methods. The mechanical properties are seen to improve significantly with the addition of the epoxy compatibilizer, approaching values close to those of virgin LDPE. The scanning electron micrographs of the compatibilized blends show ductile failure which evidently contribute to improved mechanical properties. © 2001 Society of Chemical Industry     

Optimum compatibilization for the nonflammability of thermoplasticized crosslinked polyethylene/metal hydroxides composites with a compatibilizer

Nonflammability of the thermoplasticized crosslinked polyethylene (PE)/polyolefin elastomer (POE)/metal hydroxide flame retardant/compatibilizer composites were investigated. The thermoplasticized crosslinked PE was decrosslinked from the crosslinked high‐density PE under the supercritical methanol condition. Two types of metal hydroxides: aluminum hydroxide (AH) and magnesium hydroxide (MH), and a low‐density polyethylene‐g‐maleic anhydride (LM) were used as flame retardants and a compatibilizer, respectively. Nonflammability of both PE/POE/AH/LM and PE/POE/MH/LM composites was enhanced with metal hydroxide flame retardant concentration. PE/POE/MH/LM composites had better nonflammability than PE/POE/AH/LM composites at the same flame retardant concentration. Interestingly, nonflammability of the composites was also strongly influenced by the compatibilizer concentration. At low compatibilizer concentration, the nonflammability of the PE/POE/MH/LM composites was improved with the compatibilizer concentration. In contrast, at high compatibilizer concentration, the nonflammability of the PE/POE/MH/LM composites was deteriorated with the compatibilizer concentration. This demonstrates that optimum concentration of the compatibilizer can help to enhance the efficiency of the flame retardants in the development of the nonflammable polyolefin for the wire and cable industry. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

The effects of dynamic vulcanization and compatibilizer on properties of paper sludge‐filled polypropylene/ethylene propylene diene terpolymer composites

The effects of dynamic vulcanization (DV) and dynamic vulcanization plus compatibilizer (DVC) of paper sludge (PS) filled polypropylene/ethylene propylene diene terpolymer (PP/EPDM) composites on torque development, mechanical properties, water absorption, morphology, and thermal properties were studied. Results show that DV and DVC composites exhibit higher stabilization torque than unvulcanized composites (UV). The dynamic vulcanized (DV) and dynamic vulcanized plus compatibilizer (DVC) composites exhibit higher tensile strength, elongation at break, and Young's modulus but lower water absorption than unvulcanized composites. The scanning electron microscopy (SEM) study of tensile fracture surface of DV and DVC composites shows the improved interfacial interaction between PS and PP/EPDM matrix. The DV and DVC composites also exhibit better thermal stability and higher crystallinity than unvulcanized PP/EPDM/PS composites. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effects of material parameters on the diffusion and sorption properties of wood‐flour/polypropylene composites

Composites of wood in a thermoplastic matrix (wood–plastic composites) are considered a low maintenance solution to using wood in outdoor applications. Knowledge of moisture uptake and transport properties would be useful in estimating moisture‐related effects such as fungal attack and loss of mechanical strength. Our objectives were to determine how material parameters and their interactions affect the moisture uptake and transport properties of injection‐molded composites of wood‐flour and polypropylene and to compare two different methods of measuring moisture uptake and transport. A two‐level, full‐factorial design was used to investigate the effects and interactions of wood‐flour content, wood‐flour particle size, coupling agent, and surface removal on moisture uptake and transport of the composites. Sorption and diffusion experiments were performed at 20°C and 65 or 85% relative humidity as well as in water, and diffusion coefficients were determined. The wood‐flour content had the largest influence of all parameters on moisture uptake and transport properties. Many significant interactions between the variables were also found. The interaction between wood‐flour content and surface treatment was often the largest. The diffusion coefficients derived from the diffusion experiments were different from those derived from the sorption experiments, suggesting that different mechanisms occur. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 752–763, 2007