Structure and properties of phase change materials based on HDPE,soft Fischer‐Tropsch paraffin wax,and wood flour

Phase‐change materials based on high density polyethylene (HDPE), soft Fischer‐Tropsch paraffin wax (M3), and alkali‐treated wood flour (WF) were investigated. The blend and composite samples were prepared by melt mixing using a Brabender Plastograph, followed by melt pressing. They were characterized in terms of their morphology, as well as thermal, mechanical, thermo‐mechanical, and water absorption properties. Although SEM micrographs showed some evidence of intimate contact between the WF particles and the HDPE matrix as a result of alkali treatment, poor filler dispersion, and interfacial adhesion were also observed. Partial immiscibility of the HDPE and the M3 wax was noticed, with the WF particles covered by wax. There was plasticization of the HDPE matrix by the wax, as well as partial cocrystallization, inhomogeneity and uneven wax dispersion in the polymer matrix. The HDPE/WF/M3 wax composites were more homogeneous than the blends. The presence of wax reduced the thermal stability of the blends and composites. Both the presence of M3 wax and WF influenced the viscoelastic behavior of HDPE. The HDPE/M3 wax blends showed an increase in the interfacial amorphous content as the wax content increases, which resulted in the appearance of a β‐relaxation peak. The presence of M3 wax in HDPE reduced the mechanical properties of the blends. For the composites these properties varied with WF content. An increase in wax content resulted to a decrease in water uptake by the composites, probably because the wax covered the WF particles and penetrated the pores in these particles. © 2010 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     

Synergistic compatibilization and reinforcement of HDPE/wood flour composites

Multi‐monomer grafted copolymers, high‐density polyethylene‐grafted‐maleic anhydride‐styrene (HDPE‐g‐(MAH‐St)) and polyethylene wax‐grafted‐ maleic anhydride ((PE wax)‐g‐MAH), were synthesized and applied to prepare high‐performance high‐density polyethylene (HDPE)/wood flour (WF) composites. Interfacial synergistic compatibilization was studied via the coordinated blending of high‐density polyethylene‐grafted‐maleic anhydride (MPE‐St) and polyethylene wax‐grafted‐ maleic anhydride (MPW) in the high‐density polyethylene (HDPE)/wood flour (WF) composites. Scanning electron microscopy (SEM) morphology and three‐dimensional WF sketch presented that strong interactive interface between HDPE and WF, formed by MPE‐St with high graft degree of maleic anhydride (MAH) together with the permeating effect of MPW with a low molecular weight. Experimental results demonstrated that HDPE/WF composites compatibilized by MPE‐St/MPW compounds showed significant improvement in mechanical properties, rheological properties, and water resistance than those compatibilized by MPE, MPE‐St or MPW separately and the uncompatibilized composites. The mass ratio of MPE‐St/MPW for optimizing the HDPE/WF composites was 5:1. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42958.     

Resistance of paper mill sludge/wood fiber/high‐density polyethylene composites to water immersion and thermotreatment

The disposal of paper mill sludge (PMS) is a difficult environmental problem. Thus, PMS has been used as a substitute for wood fiber (WF) to reinforce high‐density polyethylene (HDPE). In this study, we compared PMS–WF–HDPE composites with composites without PMS after water immersion and thermal treatment. Water immersion and thermal treatment were conducted at 25 and 70°C, respectively. The results show that the composites with PMS absorbed less water but lost more of their original flexural properties after immersion; thereby, their strength was compromised. These reduced mechanical properties could be partially restored after redrying. After the thermotreatment, the composites with added PMS lost their weight and flexural properties, whereas the composites without PMS gained flexural strength. The results show that the thermotreatment improved the impact strength of the composites when no more than one‐third of WF was replaced with PMS. Fourier transform infrared spectroscopy and energy‐dispersive X‐ray energy‐dispersive spectroscopy showed that the wood index of the PMS composite decreased more than the index of the non‐PMS composite, whereas the carbonyl index increased more. However, the PMS composite showed a lower increase in the total oxygen/carbon weight ratio. This study suggested that limited amounts of WF could be substituted with PMS to reinforce HDPE. However, WF–PMS–HDPE composites should not be used in hot, humid environments for long periods. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41655.     

Rheological behavior and mechanical properties of wood flour/high density polyethylene blends: Effects of esterification of wood with citric acid

This study explored the modifying effects of wood flour (WF) with citric acid (CA) on the rheological and mechanical properties of WF/high density polypropylene (HDPE) composites. WF was treated with CA, which acts a cross‐linking agent and melt‐blended with HDPE with a twin‐screw extruder. Injection molding was used to make tensile and impact tests samples. The rheological properties of the blends were characterized using a Haake microcompounder, torque‐, capillary‐, and rotational‐rheometer, respectively. Results show that the thermal stability of WF decreased after treatment. Compared with those of untreated composites, the tensile strength, elongation‐at‐break, and impact strength of the composites treated with 5% CA were reduced by 6%, 14%, and 16%, respectively. This reduction was attributed to embrittlement of WF, which may negatively influence the mechanical properties of the resulting composites. Scanning electron microscopy revealed better dispersion of CA‐treated WF in the composites than the untreated WF. For composites treated with 5% CA, the melt torque, viscosity, moduli, and shear stress decreased significantly, indicating an improvement in processibility. This improvement is attributed to uniform dispersion of the modified WF, as well as to better interfacial adhesion between WF and the matrix. Results suggest that treating WF with CA shows promise for improving the processibility of highly filled thermoplastic composites via extrusion/injection molding processing. POLYM. COMPOS., 37:553–560, 2016. © 2014 Society of Plastics Engineers     

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     

Mechanical,dynamic mechanical,and thermal characterization of fly ash and nanostructured fly ash‐waste polyethylene/high‐density polyethylene blend composites

Disposal of polyethylene used as carry bags is the greatest challenge increasing day by day. Composite materials were prepared by mixing Fly ash (FA) and nanostructured fly ash (NFA) from thermal power station as filler and blends of Waste polyethylene (WPE)(carry bags) collected from municipal solid waste (MSW) with virgin high‐density polyethylene (HDPE) as matrix. Different modifications were induced to improve the overall properties of these composites. At first, the WPE/HDPE blend matrix was modified by grafting with maleic anhydride (MA) and the composite prepared with FA/NFA. Then, the WPE/HDPE‐FA/NFA composite as a whole was treated with electron beam irradiation at 250 kGy radiation dose and finally the FA/NFA filler was treated with radiation dose of 250 kGy and the composite prepared. Significant enhancement in tensile strength, flexural strength, flexural modulus, and hardness are observed for MA modified and irradiated composites, the increase being more prominent in irradiated composites. Furthermore, an increase in storage/loss moduli with enhanced thermal stability was observed with the addition of FA/NFA and upon modifications. The analysis of the tensile fractured surfaces by scanning electron microscopy was in well correlation with the mechanical properties obtained. In summary, after analyzing the effects of the three different modifications on mechanical, dynamic mechanical and thermal properties, the irradiation on to the WPE/HDPE‐FA/NFA composites investigated was selected as the most appropriate for future applications. POLYM. COMPOS., 37:3256–3268, 2016. © 2015 Society of Plastics Engineers     

Thermal fractionation and properties of different polyethylene/wax blends

The influence of paraffin‐wax type and content on the properties of its blends with HDPE, LDPE, and LLDPE was investigated. Melt‐mixing of HDPE with wax gave rise to completely miscible blends for both 10 and 20% wax contents. A wax content of 30% gave rise to a partially miscible blend. These observations were supported by the thermal fractionation (stepwise cooling) results. Melt‐mixing of LDPE with hard paraffin wax gave rise to a partially miscible blend for all wax contents investigated, while complete miscibility was observed for the 10% oxidized hard paraffin wax containing blend. Complete miscibility was observed for all the LLDPE/A1 wax blends, with A1 wax as an oxidized hard paraffin wax. This indicates possible cocrystallization of this wax with LLDPE, which was also evident from the thermal fractionation curves. LLDPE blends with hard paraffin wax were, however, partially miscible for all wax contents. All the observations were supported by the surface free energy results. It is further clear from the thermal fractionation results that the presence of wax changed the crystallization behavior of LDPE and LLDPE. Changes in the tensile properties are explained in terms of the miscibility and proposed morphologies of the blends. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 2225–2236, 2007     

Investigation of thermally conducting phase‐change materials based on polyethylene/wax blends filled with copper particles

This article reports on the morphology, melting and crystallization behavior, thermal stability, tensile properties, and thermal conductivity of phase‐change materials (PCM) for thermal energy storage. These materials were based on a soft Fischer‐Tropsch paraffin wax (PCM) blended with low‐density polyethylene, linear low‐density polyethylene, and high‐density polyethylene. These immiscible blends were melt‐mixed with copper (Cu) microparticles (up to 15 vol %) to improve the thermal conductivity in the matrix material. The presence of the Cu microparticles in the PCMs did not significantly change the crystallization behavior, thermal stability, or tensile properties of the blend composites in comparison with the corresponding polyethylene/wax blends and polyethylene/Cu composites. The observed differences were related to the fact that the wax seemed to have a higher affinity for the Cu particles than any of the polyethylenes, and so it crystallized as a layer around the Cu particles. The thermal conductivity of the samples increased almost linearly with increasing Cu content, but the samples had slightly lower values than the corresponding polyethylene/Cu composites, probably because of the lower thermal conductivity of the wax. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Characteristics of paper mill sludge‐wood fiber‐high‐density polyethylene composites

Paper mill sludge (PMS) is a waste material from pulping. In this article it was used to replace part of a wood fiber (WF) filler to reinforce high‐density polyethylene (HDPE). The properties of the PMS/WF/HDPE composites were investigated. When half of WF was replaced with PMS, the bending strength and modulus of WF/HDPE composites decreased by 16.08% and 29.91%, respectively, but their impact strength increased by 11.31%. Dynamic mechanical analysis demonstrated that with PMS addition, the storage modulus decreased and the loss tangent increased. Although the flexural properties of the PMS/WF/HDPE composites decreased compared to WF/HDPE composite, they still had satisfactorily high strengths. The 30:30:36 PMS/WF/HDPE composite presented bending and impact strengths of 61.00 MPa and 12.11 kJ m⁻², respectively. The 50:20:26 PMS/WF/HDPE composite presented bending and impact strengths of 55.02 MPa and 10.37 kJ m⁻², respectively. Rheological test proved that substituting part of WF with PMS would not affectmanufacture processing. This study indicated that paper mill sludge could be used in wood plastic composites, which would reduce pollution from paper manufacturing. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Thermal and mechanical properties of LDPE/sisal fiber composites compatibilized with functionalized paraffin waxes

The effect of maleic anhydride‐grafted hard paraffin wax (MA‐g‐wax) and oxidized hard paraffin wax (OxWax), as possible compatibilizers, on the morphology, thermal and mechanical properties of LDPE/sisal fiber composites were examined. The differential scanning calorimetry (DSC) results show that sisal alone did not change the crystallization behavior of LDPE, while the two waxes influenced the crystallization behavior of LDPE in different ways, whether mixed with LDPE alone or in the presence of sisal. The thermal properties seem to be influenced by the fact that the waxes preferably crystallize around the short sisal fibers, and by the fact that the two waxes have different compatibilities with LDPE. The TGA results show an increase in the thermal stability of the blends in the presence of the two waxes, with LDPE/OxWax showing a more significant improvement. The presence of wax, however, reduced the thermal stability of the LDPE/sisal/wax composites. The presence of OxWax and MA‐g‐wax similarly influenced the tensile properties of the composites. Both waxes similarly improved the modulus of the compatibilized composites, but in both cases the tensile strengths were worse, probably because of a fairly weak interaction between LDPE and the respective waxes. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of microfiber reinforcement on the morphology,electrical, and mechanical properties of the polyethylene/poly(ethylene terephthalate)/carbon nanotube composites

In situ microfiber reinforced conductive polymer composites consisting of high‐density polyethylene (HDPE), poly(ethylene terephthalate) (PET), and multiwalled carbon nanotube (CNT) were prepared in a twin screw extruder followed by hot stretching of PET/CNT phase in HDPE matrix. For comparison purposes, the HDPE/PET blends and HDPE/PET/CNT composites were also produced without hot stretching. Extrusion process parameters, hot‐stretching speed, and CNT amount in the composites were kept constant during the experiments. Effects of PET content and molding temperature on the morphology, electrical, and mechanical properties of the composites were investigated. Morphological observations showed that PET/CNT microfibers were successfully formed in HDPE phase. Electrical conductivities of the microfibrillar composites were in semi‐conductor range at 0.5 wt% CNT content. Microfiber reinforcement improved the tensile strength of the microfibrillar HDPE/PET/CNT composites in comparison to that of HDPE/PET blends and HDPE/PET/CNT composites prepared without hot stretching. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

Effects of silane on the properties of wood‐plastic composites with polyethylene‐polypropylene blends as matrices

The influence of 3‐(trimethoxysilyl)propyl methacrylate and benzoyl peroxide on gel content, crystallinity, and mechanical performance of unfilled PP‐PE blends, and their composites with wood was investigated. All materials were compounded in a twin screw extruder and then injection molded. Specimens were then exposed to high‐humidity and elevated temperature in a humidity chamber to cross‐link any unhydrolyzed silane. Adding wood to the PE‐PP blends, increased premature cross‐linking but also increased gel contents. However, the gel contents of the composites were still low. The PP component did not appear to cross‐link well and our gels were almost entirely HDPE. Fourier Transfer Infrared (FTIR) spectra provided additional evidence that TMSPM is grafted and cross‐linked in unfilled PE‐PP blends. Unfortunately, the spectra of wood composites proved difficult to interpret because of the complexity and overlap of the FTIR spectra of the wood. The HDPE component annealed when exposed to high‐humidity and elevated temperature, although less so in samples with high‐gel contents, presumably because of the decreased mobility. Annealing influenced mechanical performance, especially increasing moduli. Adding peroxide and silane appeared to improve adhesion between the wood flour and matrix in the composites but had little effect on energy absorbed during high‐speed puncture tests. Published 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Thermal analysis of high‐density polyethylene and low‐density polyethylene with enhanced biodegradability

The thermal properties of high‐density polyethylene (HDPE) and low‐density polyethylene (LDPE) filled with different biodegradable additives (Mater‐Bi AF05H, Cornplast, and Bioefect 72000) were investigated with thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The DSC traces of the additives indicated that they did not undergo any significant phase change or transition in the temperature region typically encountered by a commercial composting system. The TGA results showed that the presence of the additive led to a thermally less stable matrix and higher residue percentages. The products obtained during the thermodegradation of these degradable polyolefins were similar to those from pure polyethylenes. The LDPE blends were thermally less stable than the HDPE blends. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 86: 764–772, 2002     

Blend of high‐density polyethylene and a linear low‐density polyethylene with compositional‐invariant mechanical properties

This article presents the tensile properties and morphological characteristics of binary blends of the high‐density polyethylene (HDPE) and a linear low‐density polyethylene (LLDPE). Two constituents were melt blended in a single‐screw extruder. Injection‐molded specimens were evaluated for their mechanical properties by employing a Universal tensile tester and the morphological characteristics evaluated by using a differential scanning calorimeter and X‐ray diffractometer. It is interesting to observe that the mechanical properties remained invariant in the 10–90% LLDPE content. More specifically, the yield and breaking stresses of these blends are around 80% of the corresponding values of HDPE. The yield elongation and elongation‐at‐break are around 65% to corresponding values of HDPE and the modulus is 50% away. Furthermore, the melting endotherms and the crystallization exotherms of these blends are singlet in nature. They cluster around the corresponding thermal traces of HDPE. This singlet characteristic in thermal traces entails cocrystallization between these two constituting components. The clustering of thermal traces of blends near HDPE meant HDPE‐type of crystallites were formed. Being nearly similar crystallites of blends to that of HDPE indicates nearness in mechanical properties are observed. The X‐ray diffraction data also corroborate these observations. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2604–2608, 2002     

Blends of high‐density polyethylene with chlorinated polyethylene: Morphology,thermal, rheological,and mechanical properties

Blends of high‐density polyethylene (HDPE) with chlorinated polyethylene (CPE) were generated using melt mixing. CPE of two different chlorination contents was used and its amount in the blends was varied from 1% till 30%. The rheological, thermal, mechanical, and morphological properties of the blends were characterized along with miscibility analysis. In general, better mixing of the CPE polymer in HDPE was observed at lower CPE concentration and reduced mixing or immiscibility occurred at higher concentration of CPE. However, the extent of immiscibility was different in both CPE25 and CPE35 systems. The rheological analysis of the data using Cole‐Cole, Han‐Chuang and van Gurp plots confirmed the miscibility of CPE25 blends (except for 30% CPE25 blend at lower frequency) whereas CPE35 blends with 10–30% CPE content were immiscible. Highest increase in the rheological properties (complex moduli) was observed at 2% CPE content. The mechanical properties of the CPE25 blends were superior than the corresponding CPE35 blends especially at higher CPE concentration where effects of immiscibility as well as matrix plasticization played a role. The morphology characterization using TEM indicated change in the crystalline features of the polymer in the case of CPE35 blends. The optical microscopy also confirmed the better mixing of CPE25 polymers in HDPE than CPE35. The CPE25 blends exhibited uniformly dispersed CPE phase which was also confirmed by the rheological analysis. However, the blends of CPE35 with 10% CPE content onwards had significant phase immiscibility. POLYM. ENG. SCI., 54:85–95, 2014. © 2013 Society of Plastics Engineers     

Morphological,mechanical, and physical properties of composites made with wood flour‐reinforced polypropylene/recycled poly(ethylene terephthalate) blends

Wood flour (WF)‐filled composites based on a polypropylene (PP)/recycled polyethylene terephthalate (r‐PET) matrix were prepared using two‐step extrusion. Maleic anhydride grafted polypropylene (MAPP) was added to improve the compatibility between polymer matrices and WF. The effects of filler and MAPP compatibilization on the water absorption, mechanical properties, and morphological features of PP/r‐PET/WF composites were investigated. The addition of MAPP significantly improved mechanical properties such as tensile strength, flexural strength, tensile modulus, and flexural modulus compared with uncompatibilized composites, but decreased elongation at break. Scanning electron microscopic images of fracture surface specimens revealed better interfacial interaction between WF and polymer matrix for MAPP‐compatibilized PP/r‐PET/WF composites. MAPP‐compatibilized PP/r‐PET/WF composites also showed reduced water absorption due to improved interfacial bonding, which limited the amount of absorbable water molecules. These results indicated that MAPP acts as an effective compatibilizer in PP/r‐PET/WF composites. POLYM. COMPOS., 38:1749–1755, 2017. © 2015 Society of Plastics Engineers     

Influence of fly ash cenospheres on performance of coir fiber‐reinforced recycled high‐density polyethylene biocomposites

Recycled high‐density polyethylene (RHDPE)/coir fiber (CF)‐reinforced biocomposites were fabricated using melt blending technique in a twin‐screw extruder and the test specimens were prepared in an automatic injection molding machine. Variation in mechanical properties, crystallization behavior, water absorption, and thermal stability with the addition of fly ash cenospheres (FACS) in RHDPE/CF composites were investigated. It was observed that the tensile modulus, flexural strength, flexural modulus, and hardness properties of RHDPE increase with an increase in fiber loading from 10 to 30 wt %. Composites prepared using 30 wt % CF and 1 wt % MA‐g‐HDPE exhibited optimum mechanical performance with an increase in tensile modulus to 217%, flexural strength to 30%, flexural modulus to 97%, and hardness to 27% when compared with the RHDPE matrix. Addition of FACS results in a significant increase in the flexural modulus and hardness of the RHDPE/CF composites. Dynamic mechanical analysis tests of the RHDPE/CF/FACS biocomposites in presence of MA‐g‐HDPE revealed an increase in storage (E′) and loss (E″) modulus with reduction in damping factor (tan δ), confirming a strong influence between the fiber/FACS and MA‐g‐HDPE in the RHDPE matrix. Differential scanning calorimetry, thermogravimetric analysis thermograms also showed improved thermal properties in the composites when compared with RHDPE matrix. The main motivation of this study was to prepare a value added and low‐cost composite material with optimum properties from consumer and industrial wastes as matrix and filler. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42237.     

Studies on the physico‐mechanical,thermal, and morphological behaviors of high density polyethylene/coleus spent green composites

This study is aimed at utilizing nutraceutical industrial waste and reducing carbon footprints of plastics. Eco‐friendly “green composites” of high density polyethylene (HDPE) were fabricated using coleus spent (CS)—a nutraceutical industrial waste as reinforcing filler and maleic anhydride‐graft‐polyethylene (MA‐g‐PE) as compatibilizer. Composites were fabricated with 5, 10, 15, and 20% (w/w) of CS by extrusion method. The fabricated HDPE/CS composites were evaluated for mechanical and thermal behavior. A slight improvement of about 5% in tensile strength and marked improvement of about 25% in tensile modulus for 20 wt % CS filled HDPE composites was noticed. The effect of CS content on rheological behavior was also studied. Thermal characteristics were performed using thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). TGA thermogram indicated increased thermal stability of CS‐filled composites. From TGA curves the thermal degradation kinetic parameters of the composites have been calculated using Broido's method. The enthalpy of melting (ΔH_m) obtained from DSC curves was reduced with increase in CS content in HDPE matrix, due to decrease in HDPE content in composite systems. An increase in CS loading increased the water absorption behavior of the composites slightly. Morphological behavior of cryo‐fractured composites has been studied using scanning electron microscopy. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Viscoelastic,thermal, and morphological analysis of HDPE/EVA/CaCO<Subscript>3</Subscript> ternary blends

High density polyethylene (HDPE), calcium carbonate (CaCO₃), and ethylene vinyl acetate (EVA) ternary reinforced blends were prepared by melt blend technique using a twin screw extruder. The thermal properties of these prepared ternary blends were investigated by differential scanning calorimetry. The effect of EVA loading on the melting temperature (T _m) and the crystallization temperature (T _C) was evaluated. It was found that the expected heterogeneous nucleating effect of CaCO₃ was hindered due to the presence of EVA. The melt viscosities of the ternary reinforced blends were affected by the % loading of CaCO₃, EVA, and vinyl acetate content. Viscoelastic analysis showed that there is a reduction of the storage modulus (G′) with increasing of EVA loading as compared to neat HDPE resin or to HDPE/CACO₃ blends only. The morphology of the composites was characterized by scanning electron microscopy (SEM). The dispersion and interfacial interaction between CaCO₃ with EVA and HDPE matrix were also investigated by SEM. We observed two main types of phase structures; encapsulation of the CaCO₃ by EVA and separate dispersion of the phases. Other properties of ternary HDPE/CaCO₃/EVA reinforced blends were investigated as well using thermal, rheological, and viscoelastic techniques.