Characterization of bio‐filler derived from seashell wastes and its effect on the mechanical,thermal, and flame retardant properties of ABS composites

The seashell is mainly composed of calcium carbonate and organic materials which, when decompose, produce harmful gases with significant odor and toxicity. Therefore, their wastes are considered to be a problem and could be hazardous to human. To overcome this problem, this study proposed to use grinded seashell wastes (SS) as a bio‐filler to reinforce acrylonitrile–butadiene–styrene copolymer (ABS). Commercial calcium carbonate, CaCO₃ (CC) was also used to compare the results. The filler and their composites were characterized by X‐ray Fluorescence (XRF), X‐ray Diffraction (XRD), Fourier Transform Infrared spectroscopy (FT‐IR), Scanning Electron Microscopy (SEM), Dynamic Mechanical Analysis (DMA), Thermogravimetric Analysis (TGA), and Cone Calorimeter. DMA data show that the addition of low amounts of seashell bio‐filler to ABS increases the storage modulus (E ′). The glass transition temperature (T _g) values are shifted to higher temperature. On the other hand, the ABS/SS composite shows a higher tensile strength than CC filled ABS. TGA results exhibit that there is an enhancement in the thermal stability when calcium carbonate from seashell is added. Good flame retardant properties were achieved with increasing the bio‐filler content. According to XRD and FT‐IR results of the char residues after cone calorimetric tests, the compact char layer acts as a barrier to oxygen and heat transfer, preventing the escape of polymer fragments to the gas phase, and decreasing the heat release rate during combustion. POLYM. COMPOS., 38:2788–2797, 2017. © 2015 Society of Plastics Engineers     

Forest‐based resources as fillers in biobased polyurethane foams

Six fillers from forestry wastes (wood, bark, cones and needles from young pine trees, kraft lignin, and recycled paper sludge from industry wastes) were incorporated into polyurethane (PU)‐based foams prepared via free‐rise pouring method. Variable filler contents (1, 5, and 10 wt %) and NCO/OH ratios (0.6, 0.9, and 1.2) were investigated. A simple mixture (1:3) of castor oil and crude glycerin (byproduct from biodiesel production) was used as biobased polyol. The foam composites were investigated through spectroscopy, morphological, mechanical, and hygroscopic analyses. The addition of fillers decreased water uptake and yielded rigid PU systems with more homogenous cell structure. The 1% and 5% reinforcement wood were the most effective among the studied compositions, with better mechanical and hygroscopic performance, probably due the higher compatibility of the wood with the PU system, which promote urethanic bonds between filler and isocyanate, as indicated by wet chemical results and micrographs. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45684.     

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     

Simultaneous full‐interpenetrating polymer networks of blocked polyurethane and vinyl ester. II. Static and dynamic mechanical properties

Simultaneous full‐interpenetrating polymer networks (full‐IPNs) based on blocked polyurethane (PU) and vinyl ester (VE) have been prepared. The static and dynamic properties of these IPNs have been examined. Results show that the tensile strength and flexural strength of IPNs increased with blocked PU content to a maximum value at 7.5 wt % PU content and then decreased. The tensile modulus, flexural modulus, and hardness of IPNs decreased with increasing blocked PU content. The impact strength of IPNs increased with increasing blocked PU content. The tensile strength, flexural strength, tensile modulus, and flexural modulus of IPNs increased with filler (kaolin) content to a maximum value at 20 to 25 phr filler content and then decreased. The higher the filler content, the greater the hardness, and the lower the impact strength of IPNs. The tensile strength, flexural strength, tensile modulus, flexural modulus, and hardness of IPNs increased with increasing VE initiator content. The dynamic technique was used to determined the damping behavior across a temperature range. Results show that the glass transition temperature (T_g) of IPNs are shifted inwardly compared with pure PU and VE, which indicated that the blocked PU–VE IPNs showed excellent compatible. Meanwhile, the glass transition temperature was shifted to a higher temperature with increased filler content. The dynamic storage modulus (E′) of IPNs increased with increasing VE and filler content. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 71: 1977–1985, 1999     

Effects of filler–filler and polymer–filler interactions on rheological and mechanical properties of HDPE–wood composites

High‐density polyethylene (HDPE)–wood composite samples were prepared using a twin‐screw extruder. Improved filler–filler interaction was achieved by increasing the wood content, whereas improved polymer–filler interaction was obtained by adding the compatibilizer and increasing the melt index of HDPE, respectively. Then, effects of filler–filler and polymer–filler interactions on dynamic rheological and mechanical properties of the composites were investigated. The results demonstrated that enhanced filler–filler interaction induced the agglomeration of wood particles, which increased the storage modulus and complex viscosity of composites and decreased their tensile strength, elongation at break, and notched impact strength because of the stress concentration. Stronger polymer–filler interaction resulted in higher storage modulus and complex viscosity and increased the tensile and impact strengths due to good stress transfer. The main reasons for the results were analyzed. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Mechanical and Morphological Studies of Rubber Wood Sawdust-Filled UPR Composite Based on Recycled PET

Rubber wood sawdust fillers were mixed with unsaturated polyester matrix, which was prepared by recycling of PET waste from soft drink bottles, to prepare rubber wood sawdust/UPR composite. PET wastes were subjected to recycle by glycolysis and depolymerized to its monomer and dimmer. The glycolysed product was used to prepare unsaturated polyester resin. The FTIR analysis has been done on the resin and the glycolysed product. The resin then mixed with rubber wood sawdust fillers before and after alkali treatment with 10% NaOH. The effect of surface treatment and filler content on the mechanical properties and water absorption of the composite were studied. The tensile fractured surfaces of the composites were studied by Scanning Electron Microscopic (SEM) technique to investigate the interfacial bonding between the matrix and the filler. The results show that the tensile modulus increased with increasing filler contents. In addition, the results show that alkali treatment causes a better adhesion between rubber wood sawdust and UPR matrix and improves the mechanical properties.     

Valorization of waste thermoset material as a filler in thermoplastic: Mechanical properties of phenolic molding compound waste‐filled PP composites

As most thermoset material, phenolic molding compound (PMC) wastes are an environmental problem. Very few recycling solutions have been proposed so far for this type of material. A mechanical recycling method to valorize these materials is proposed in this work. It relies on the use of phenolic waste as filler in thermoplastic. Such phenolic filler can increase mechanical properties (tensile, flexural) of the matrix, and be used in substitution of traditional particulate fillers such as calcium carbonate or talc. In this study, several morphological parameters influencing the final mechanical properties of a PMC‐filled polypropylene (PP) micro‐composite are studied, such as filler loading rate, particles size distribution of the filler, and interfacial adhesion between the filler and the matrix. Some structural parameters are also studied and linked with mechanical properties, such as dispersion of the filler and crystallinity of the matrix. Finally, the properties of PMC‐filled PP are compared with CaCO₃‐ and talc‐filled PP. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45849.     

Use of construction and demolition wastes as mineral fillers in hybrid wood–polymer composites

The recycling of construction materials has been the subject of much research in past years. In this study, the use of construction and demolition wastes (CDWs) as mineral fillers in hybrid wood–polymer composites was studied. Two types of waste materials were used as fillers in the composites: (1) a mixture consisting of waste mineral wool (MW) and plasterboard (PB) and (2) mixed CDWs. The performance of the composites was evaluated from their mechanical properties and water‐absorption behavior. We found in the study that the addition of mineral fillers decreased the flexural strength and modulus values of the wood–polypropylene (PP) composites. On the other hand, the exchange of part of the wood with a mineral filler resulted in an increase in the impact strength of the composite. The composite manufactured with the combination of MW and PB had the lowest water absorption. The decrease in wood loading resulted in improved dimensional stability in the hybrid wood–mineral filler–PP composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43412.     

Tensile modulus modeling of carbon black/polycarbonate,carbon nanotube/polycarbonate,and exfoliated graphite nanoplatelet/polycarbonate composites

Conductive fillers are often added to thermoplastic polymers to increase the resulting composite's electrical conductivity (EC) which would enable them to be used in electrostatic dissipative and semiconductive applications. The resulting composite also exhibits increased tensile modulus. The filler aspect ratio plays an important role in modeling composite EC, and tensile modulus. It is difficult to measure the filler aspect ratio after the manufacturing process (often extrusion followed by injection molding) in the composite, especially when nanomaterials are used. The EC percolation threshold is a function of the filler aspect ratio; hence, knowledge of this percolation threshold provides a means to extract the filler aspect ratio. In this study, the percolation threshold of the composite was determined from EC measurements and modeling, which in turn was used to determine the filler aspect ratio for tensile modulus modeling. Per the authors' knowledge, this approach has not been previously reported in the open literature. The fillers; carbon black (CB: 2–10 wt %), multiwalled carbon nanotubes (CNT: 0.5–8 wt %), or exfoliated graphite nanoplatelets (GNP: 2–12 wt %); were added to polycarbonate (PC) and the resulting composites were tested for EC and tensile modulus. With the filler aspect ratio determined from EC values for CNT/PC and GNP/PC composites, the three‐dimensional randomly oriented fiber Halpin‐Tsai model accurately estimates the tensile modulus for the CNT/PC composites and the Nielsen model predicts the tensile modulus well for the CB/PC and GNP/PC composites. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

More wear‐resistant and ductile UHMWPE composite prepared by the addition of radiation crosslinked UHMWPE powder

Radiation crosslinked ultrahigh molecular weight polyethylene (X‐UHMWPE) powder was prepared by γ‐ray irradiation under nitrogen atmosphere with a dose of 50–200 kGy at a dose rate of 7 kGy/h and further annealing in vacuum at 120 °C for 4 h. The crosslinked powder was characterized by FT‐IR spectroscopy, gel content, and hot‐press molding. Then, X‐UHMWPE was added to pristine UHMWPE to prepare a composite with 0–25 wt % filler. The morphology, wear resistance, and tensile property of the composite were investigated. Using X‐UHMWPE as a filler could sufficiently improve the wear resistance of the composite. Adding 25 wt % X‐UHMWPE (dose: 150 kGy) improved wear resistance by 130% and retained approximately 90% tensile strength and 70% ductility. Wear‐resistant and ductile UHMWPE composite may be potentially used for artificial joint replacement and engineering devices. The proposed route is useful in fabricating UHMWPE material with excellent comprehensive performance or functional polymer composite. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44643.     

Preparation of a functional reduced graphene oxide and carbon nanotube hybrid and its reinforcement effects on the properties of polyimide composites

The homogeneous dispersion and strong interfacial interactions of carbon nanomaterials are vital factors on enhancing the properties of polymer composites. Two‐dimensional reduced graphene oxide (rGO) and one‐dimensional carbon nanotubes (CNTs) were first grafted by 4,4′‐oxydianiline (ODA). The successful grafting of ODA onto the rGO and CNTs were confirmed by Fourier transform infrared spectroscopy, thermogravimetric analysis, and X‐ray photoelectron spectroscopy. The hybrid carbon nanomaterials of the functionalized CNTs and rGO with different ratios were prepared via a solution‐mixing method, and their dispersion state was investigated. The hybrid carbon nanomaterials with good stability were introduced to polyimide (PI) via in situ polymerization. The morphology and properties of the polymer composites were studied. The results show that much better mechanical and electrical properties of the composites could be achieved in comparison with those of the neat PI. An improvement of 100.7% on the tensile strength and eight orders for the electrical conductivity were achieved at only a 1.0 wt % hybrid content. A significant enhancement effect was attributed to the homogeneous dispersion of the filler, filler–matrix strong interfacial interactions, and unique structure of the hybrid carbon nanomaterials in the composites. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44575.     

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.     

Fabrication of alumina based electrically conductive polymer composites

Novel electrically conductive composites were synthesized by incorporating Cu coated alumina (Cu‐Al₂O₃) powder prepared via electroless plating technique as filler (0–21wt %) into polystyrene‐b‐methylmethacrylate (PS‐b‐PMMA) and polystyrene (PS) matrices. XRD analysis depicted maximum Cu crystallite growth (26.116 nm～ plating time 30 min) onto Al₂O₃ along with a significant change in XRD patterns of composites with Cu‐Al₂O₃ inclusion. SEM–EDX analyses exhibited uniform Cu growth onto Al₂O₃ and confirmed presence of Cu, Al, Pd in Cu‐Al₂O₃, and C, O, Al, Cu, and Pd in PS‐b‐PMMA and PS composites. Increasing filler loadings exhibited increased electrical conductivity (5.55 × 10^?5S/cm for PS‐b‐PMMA; 5.0 × 10^?6S/cm for PS) with increased Young's modulus (1122MPa for PS‐b‐PMMA; 1053.9MPa for PS) and tensile strength (27.998MPa for PS‐b‐PMMA; 30.585MPa for PS) and decreased % elongation. TGA demonstrated increased thermal stability and DTG revealed two‐step degradation in composites while DSC depicted pronounced increment in T_g of Cu‐Al₂O₃/PS‐b‐PMMA with increased filler loading. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42939.     

Preparation and properties of plasticized starch/multiwalled carbon nanotubes composites

In this work we have studied the utilization of multiwalled carbon nanotubes (MWCNTs) as filler‐reinforcement to improve the performance of plasticized starch (PS). The PS/MWCNTs nanocomposites were successfully prepared by a simple method of solution casting and evaporation. The morphology, thermal behavior, and mechanical properties of the films were investigated by means of scanning electron microscopy, wide‐angle X‐ray diffraction, differential scanning calorimetry, and tensile testing. The results indicated that the MWCNTs dispersed homogeneously in the PS matrix and formed strong hydrogen bonding with PS molecules. Compared with the pure PS, the tensile strength and Young's modulus of the nanocomposites were enhanced significantly from 2.85 to 4.73 MPa and from 20.74 to 39.18 MPa with an increase in MWCNTs content from 0 to 3.0 wt %, respectively. The value of elongation at break of the nanocomposites was higher than that of PS and reached a maximum value as the MWCNTs content was at 1.0 wt %. Besides the improvement of mechanical properties, the incorporation of MWCNTs into the PS matrix also led to a decrease of water sensitivity of the PS‐based materials. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effect of filler content on the structure‐property behavior of poly(ethylene oxide) based polyurethaneurea‐silica nanocomposites

Poly(ethylene oxide) (PEO) based polyurethaneurea‐silica nanocomposites were prepared by solution blending and characterized by Fourier Transform Infrared Spectroscopy, Scanning Electron Microscopy, Differential Scanning Calorimetry and tensile testing. The colloidal silica nanoparticles with an average size of 50 nm were synthesized by modified Stöber method in isopropanol. Silica particles were incorporated into three cycloaliphatic polyurethaneurea (PUs) copolymers based on PEO oligomers with molecular weights of 2,000, 4,600, and 8,000 g/mol. Hard segment content of PUs was constant at 30% by weight. Silica content of the PU nanocomposites varied between 1 and 20% by weight. Soft segment (SS) glass transition and melting temperatures slightly increased with increasing filler content for all the copolymers. Degree of SS crystallinity first increased with 1% silica incorporation and subsequently decreased by further silica addition. Elastic modulus and tensile strengths of PU copolymers gradually increased with increasing amount of the silica filler. Elongation at break values gradually decreased in PEO‐2000 based PU copolymer with increasing silica content, whereas no significant change was observed in PUs based on PEO‐4600 and PEO‐8000. Enhancement in tensile properties of the materials was mainly attributed to the homogeneous distribution of silica filler in polymer matrices and strong polymer‐filler interactions. POLYM. ENG. SCI., 58:1097–1107, 2018. © 2017 Society of Plastics Engineers     

Calcium carbonate and wood reinforced hybrid PVC composites

In this article, poly(vinyl chloride) (PVC) sandwich‐structured hybrid composites with amorphous calcium carbonate and wood‐filled cores were obtained by compression molding. It has been determined that wood addition up to a weight ratio of 33% reported to the total filler amount is beneficial in improving both the inter‐filler and filler‐matrix interfacial adhesion, which alongside with the promoting of the amorphous PVC matrix crystallization is responsible for an increase up to 34% in the flexural strength of the composites, compared to unfilled PVC. The hybrid filled composites present up to 35% lower friction coefficients and up to 20% higher Brinell hardness values than the composites filled with calcium carbonate alone. Subsequently, wood addition determines an increase in the oxidation onset temperature for PVC and an increase with up to 20% in the sound and thermal‐insulative properties of the composites, compared to unfilled PVC. The dominating dispersive part of the composites surface energy aids in improving the mass and dimensional stability of the assembly to both water and dilute hydrochloric acid aqueous solutions. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46317.     

Synergistic effect of expandable graphite and melamine phosphate on flame‐retardant polystyrene

The halogen‐free flame‐retardant polystyrene (PS) composites containing expandable graphite (EG) and melamine phosphate (MP) were prepared successfully, and the thermal degradation behavior and fire performance were investigated by various measurements. The experimental results show that EG and MP have a synergistic effect on flame‐retardant PS, which can catalyze the char formation from PS. PS/MP/EG_(1:2) composite achieves limited oxygen index value of 28.0% and UL‐94V‐0 (1.6 mm) rate. The mass retention at high temperature (800 °C) under air atmosphere of PS composites have a large increase by the introduction of EG and MP. Microscale combustion calorimeter (MCC) and cone calorimetric analysis indicate that the heat release rate and total heat release of PS/MP/EG_(1:2) composite are reduced significantly, because the formed thick char layer has a notable barrier property. The study on the char residue of PS/MP/EG_(1:2) composite by X‐ray photoelectron spectroscopy (XPS) analysis confirms the formation of the stable structures containing P? O? C. Furthermore, the mechanical properties of PS composites were also investigated; compared with neat PS, the addition of flame retardants leads to the decrease of tensile strength and flexural strength, but the impact strength of PS/MP/EG_(1:2) has increased by 44.2%. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45474.     

Pea starch‐based composite films with pea hull fibers and pea hull fiber‐derived nanowhiskers

New applications of both pea hull fiber (PHF) and PHF‐derived nanowhiskers (PHFNW), isolated from PHF by acid‐hydrolysis, as fillers in starch‐based biocomposite films were explored in this work. Two series of films were prepared by blending pea starch (PS), respectively, with PHF and PHFNW. The effects of PHF and PHFNW as filler on the structure and properties of the composite films were comparatively investigated by observation of morphology and analysis of thermal, optical, and mechanical properties. The results revealed that the PS/PHFNW nanocomposite films exhibited improved physical properties over both the neat PS film and PS/PHF microcomposite films. The light transmittance at 800 nm, tensile strength, elongation at break, and Young's modulus were 56.0%, 4.1 MPa (Megapascal), 30.1%, 40.3 MPa, respectively, for the PS film without filler; 58.0%, 7.6 MPa, 41.8%, and 415.2 MPa for the PS/PHFNW film containing 10 wt% filler; and 37.2%, 2.8 MPa, 17.0%, and 29.8 MPa for the PS/PHF film containing 10 wt% filler. The improvement to the properties of PS/PHFNW nanocomposite films may be attributed to the nanometer size effect of PHFNW, which resulted in the homogeneous dispersion of PHFNW within the PS, and the strong interactions between the matrix and the nanoscale filler. POLYM. ENG. SCI., 2009. Published by the Society of Plastics Engineers     

Preparation of HDPE/SEBS‐g‐MAH and its effect on mechanical properties of HDPE/wood flour composites

In this article, high density polyethylene/styrene‐ethylene‐butylene‐styrene block copolymer blends (HDPE/SEBS) grafted by maleic anhydride (HDPE/SEBS‐g‐MAH), which is an effective compatibilizer for HDPE/wood flour composites was prepared by means of torque rheometer with different contents of maleic anhydride (MAH). The experimental results indicated that MAH indeed grafted on HDPE/SEBS by FTIR analysis and the torque increased with increasing the content of maleic anhydride and dicumyl peroxide (DCP). Styrene may increase the graft reaction rate of MAH and HDPE/SEBS. When HDPE/SEBS MAH was added to HDPE/wood flour composites, tensile strength and flexural strength of composites can reach 25.9 and 34.8 MPa in comparison of 16.5 and 23.8 MPa (without HDPE/SEBS‐g‐MAH), increasing by 157 and 146%, respectively. Due to incorporation of thermoplastic elastomer in HDPE/SEBS‐g‐MAH, the Notched Izod impact strength reached 5.08 kJ m^?2, increasing by 145% in comparison of system without compatibilizer. That HDPE/SEBS‐g‐MAH improved the compatibility was also conformed by dynamic mechanical measurement. Scanning electron micrographs provided evidence for strong adhesion between wood flour and HDPE matrix with addition of HDPE/SEBS‐g‐MAH. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Tensile modulus of polymer/CNT nanocomposites containing networked and dispersed nanoparticles

The properties of three‐dimensional networks of nanoparticles in polymer/carbon nanotubes (CNT) nanocomposites (PCNT) are particularly interesting from fundamental and application views. In this article, a new model is suggested for predicting the tensile modulus of PCNT using the Ouali and Paul models. The Ouali model considers the network of CNT in a polymer matrix, while the Paul model predicts the tensile modulus of samples containing dispersed nanoparticles. The predictions of the suggested approach are compared with experimental data from several samples. Also, the roles of the main parameters in the tensile modulus of PCNT are evaluated. The predictions agree with the experimental results at different filler concentrations. The roles of these parameters on the tensile modulus of PCNT are discussed based on the properties of CNT networks. © 2017 American Institute of Chemical Engineers AIChE J, 63: 220–225, 2018