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     

Preparation and properties of biocomposites composed of glycerol‐based epoxy resins,tannic acid,and wood flour

After polyglycerol polyglycidyl ether (PGPE) and glycerol polyglycidyl ether (GPE) were mixed with tannic acid (TA) in ethanol and without solvent at epoxy/hydroxyl ratio 1/1, the obtained GPE‐TA and PGPE‐TA solutions were mixed with wood flour (WF), prepolymerized at 50°C, and subsequently compressed at 160°C for 3 h to give GPE‐TA/WF and PGPE‐TA/WF biocomposites with WF content 50–70 wt %, respectively. The storage moduli of the biocomposites in the rubbery state at more than 80°C were much higher than that of the control cured resins. The PGPE‐TA/WF composites had higher tensile modulus and rather lower tensile strength than PGPE‐TA. On the other hand, both the tensile modulus and strength of GPE‐TA/WF were much higher than those of GPE‐TA (2.4 GPa and 37 MPa). Those values of GPE‐TA/WF increased with WF content, became maximal values (5.1 GPa and 51 MPa) at WF content 60 wt %, and were lowered at 70 wt %. FE‐SEM analysis of the fractured surface of the biocomposites revealed that WF is tightly incorporated into the crosslinked epoxy resins. As a result of optimization of the epoxy/hydroxyl molar ratio for GPE‐TA/WF composite with WF content 60 wt %, the composite prepared at the ratio of 1.0/0.8 showed the highest tensile modulus and strength. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Thermal conductivity and dynamic mechanical property of glycidyl methacrylate‐grafted multiwalled carbon nanotube/epoxy composites

The well dispersed multiwalled carbon nanotube (MWCNT)/epoxy composites were prepared by functionalization of the MWCNT surfaces with glycidyl methacrylate (GMA). The morphology and thermal properties of the epoxy nanocomposites were investigated and compared with the surface characteristics of MWCNTs. GMA‐grafted MWCNTs improved the dispersion and interfacial adhesion in epoxy resin, and enhanced the network structure. The storage modulus of 3 phr GMA‐MWCNTs/epoxy composites at 50°C increased from 0.32 GPa to 2.87 GPa (enhanced by 799%) and the increased tanδ from 50.5°C to 61.7°C (increased by 11.2°C) comparing with neat epoxy resin, respectively. Furthermore, the thermal conductivity of 3 phr GMA‐MWCNTs/epoxy composite is increased by 183%, from 0.2042 W/mK (neat epoxy) to 0.5781 W/mK. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation and properties of bio‐based epoxy montomorillonite nanocomposites derived from polyglycerol polyglycidyl ether and ε‐polylysine

Glycerol polyglycidyl ether (GPE) and polyglycerol polyglycidyl ether (PGPE) were cured with ε‐poly(L ‐lysine) (PL) using epoxy/amine ratios of 1 : 1 and 2 : 1 to create bio‐based epoxy cross‐linked resins. When PGPE was used as an epoxy resin and the epoxy/amine ratio was 1 : 1, the cured neat resin showed the greatest glass transition temperature (T_g), as measured by differential scanning calorimetry. Next, the mixture of PGPE, PL, and montomorillonite (MMT) at an epoxy/amine ratio of 1 : 1 in water was dried and cured finally at 110°C to create PGPE‐PL/MMT composites. The X‐ray diffraction and transmission electron microscopy measurements revealed that the composites with MMT content 7–15 wt % were exfoliated nanocomposites and the composite with MMT content 20 wt % was an intercalated nanocomposite. The T_g and storage modulus at 50–100°C for the PGPE‐PL/MMT composites measured by DMA increased with increasing MMT content until 15 wt % and decreased at 20 wt %. The tensile strength and modulus of the PGPE‐PL/MMT composites (MMT content 15 wt %: 42 and 5300 MPa) were much greater than those of the cured PGPE‐PL resin (4 and 6 MPa). Aerobic biodegradability of the PGPE‐PL in an aqueous medium was ～ 4% after 90 days, and the PGPE‐PL/MMT nanocomposites with MMT content 7–15 wt % showed lower biodegradability. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Preparation and properties of biocomposites composed of epoxidized soybean oil,tannic acid,and microfibrillated cellulose

As a new biobased epoxy resin system, epoxidized soybean oil (ESO) was cured with tannic acid (TA) under various conditions. When the curing conditions were optimized for the improvement of the thermal and mechanical properties, the most balanced properties were obtained when the system was cured at 210°C for 2 h at an epoxy/hydroxyl ratio of 1.0/1.4. The tensile strength and modulus and tan δ peak temperature measured by dynamic mechanical analysis for the ESO–TA cured under the optimized condition were 15.1 MPa, 458 MPa, and 58°C, respectively. Next, we prepared biocomposites of ESO, TA, and microfibrillated cellulose (MFC) with MFC contents from 5 to 11 wt % by mixing an ethanol solution of ESO and TA with MFC and subsequently drying and curing the composites under the optimized conditions. The ESO–TA–MFC composites showed the highest tan δ peak temperature (61°C) and tensile strength (26.3 MPa) at an MFC content of 9 wt %. The tensile modulus of the composites increased with increasing MFC content and reached 1.33 GPa at an MFC content of 11 wt %. Scanning electron microscopy observation revealed that MFC was homogeneously distributed in the matrix for the composite with an MFC content of 9 wt %, whereas some aggregated MFC was observed in the composite with 11 wt % MFC. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Polyethylene/boron nitride composites for space radiation shielding

Composites made with boron might be absorbers of low energy neutrons, and could be used for structural materials for spacecraft. Polyethylene/boron nitride composites were fabricated using conventional polymer processing techniques, and were evaluated for mechanical and radiation shielding properties. The boron nitride powder surfaces were also functionalized to improve interfacial adhesion. Addition of neat boron nitride to an injection molding grade HDPE increased the tensile modulus from 588 to 735 MPa with 15 vol % filler. The bonding of a trifunctional alkoxysilane to the powder surface prior to processing increases the composite modulus to 856 MPa at the same loading. Scanning electron microscopy of fracture surfaces verified that the silane‐treated powders had improved adhesion at the filler/polymer interface. Radiation shielding measurements of a 2 wt % boron nitride composite were improved over those of the neat polyethylene. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Synthesis and characterization of chlorinated soy oil based epoxy resin/glass fiber composites

Composites with good toughness properties were prepared from chemically modified soy epoxy resin and glass fiber without additional petroleum based toughening agent. Chlorinated soy epoxy (CSE) resin was prepared from soybean oil. The CSE was characterised by spectral, and titration method. The prepared CSE was blended with commercial epoxy resin in different ratios and cured at 85°C for 3 h, and post cured at 225°C for 2 h using m‐phenylene diamine (MPDA) as curing agent. The cure temperatures of epoxy/CSE/MPDA with different compositions were found to be in the range of (151.2–187.5°C). The composite laminates were fabricated using epoxy /CSE/MPDA‐glass fiber at different compositions. The mechanical properties such as tensile strength (248–299 MPa), tensile modulus (2.4–3.4 GPa), flexural strength (346–379 MPa), flexural modulus (6.3–7.8 GPa) and impact strength (29.7–34.2) were determined. The impact strength increased with the increase in the CSE content. The interlaminor fracture toughness (G_IC) values also increased from 0.6953 KJ/m² for neat epoxy resin to 0.9514 KJ/m² for 15%CSE epoxy‐modified system. Thermogravimetric studies reveal that the thermal stability of the neat epoxy resin was decreased by incorporation of CSE. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Physico‐mechanical,thermal, and coating properties of composite materials prepared with epoxy resin/steel slag

The interest in using different solid waste as reinforcement in polymer composite preparation has increased considerably in recent years. Slag is one of the inorganic waste materials obtained from ore processing. In this work, epoxy composites filled with different percentages of slag were prepared. Physico‐mechanical, thermal, and coating properties of these composites were determined depending on the amount of filler, type of hardener, and polyethylene glycol (PEG) addition. X‐ray diffraction (XRD) studies were carried out to examine the compatibility of the filler and epoxy resin and XRD results showed good compatibility between two materials. The results of mechanical testing illustrated that hardness of the epoxy composites containing anhydride was partially higher than with Epamine PC17 in contrast to elongation at break. The tensile strength and Young modulus decreased with increasing filler amount. When compared to neat epoxy resin, corrosion, and adhesion properties of the composites with filler addition did not change significantly. The highest water sorption values were obtained for the epoxy composites with PEG addition. The composites hardened by anhydride had better thermal stability than the composites including Epamine PC17. POLYM. COMPOS., 38:1974–1981, 2017. © 2015 Society of Plastics Engineers     

Creep and relaxation behavior of woven glass/epoxy substrates for multilayer circuit board applications

The creep behavior of a common woven glass/epoxy composite substrate for multilayer circuit board applications was characterized using dynamic mechanical analysis (DMA). The creep compliance was measured in both the warp and fill directions of the composite over a temperature range of 30°C to 155°C. The creep compliance of the neat FR-4 epoxy matrix was also characterized for comparison with the composite response. Master creep curves were obtained for the neat resin and the composite in the warp and fill directions assuming thermorheologically simple behavior and applying the time-temperature superposition principle. The creep data was fit to a Prony series and then converted to relaxation data in the Laplace domain. Micromechanical models were developed to predict the relaxation behavior of the woven glass/epoxy composite from the elastic properties and the geometry of the glass fabric and relaxation behavior of the neat resin. Model predictions were compared with experimental data.     

Cellulose NANOFIBER‐polyethylene nanocomposites modified by polyvinyl alcohol

The uniform dispersion of cellulose nanofibers (CNFs) in non‐polar polymer matrices is a primary problem to overcome in creating novel nanocomposites from these materials. The aim of this study was to produce CNF‐polyethylene (PE) nanocomposites by melt compounding followed by injection molding to investigate the possibility of using polyvinyl alcohol (PVA) to improve the dispersion of CNF in the PE matrix. The tensile strength of CNF‐ filled composites was 17.4 MPa with the addition of 5 wt % CNF–PVA, which was 25% higher than the strength of neat PE. The tensile modulus of elasticity increased by 40% with 5% CNF–PVA addition. Flexural properties also significantly increased with increased CNF loading. Shear viscosity increased with increasing CNF content. The elastic moduli of the PE/CNF composites from rheological measurements were greater than those of the neat PE matrix because of the intrinsic rigidity of CNF. Melt creep compliance decreased by about 13% and 45% for the composites with 5 wt % CNF and 10 wt % CNF, respectively. It is expected that the PVA carrier system can contribute to the development of a process methodology to effectively disperse CNFs containing water in a polymer matrix. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 42933.     

Mechanical and thermal properties of poly(butylene succinate)/plant fiber biodegradable composite

Biodegradable polymeric composites were fabricated from poly(butylene succinate) (PBS) and kenaf fiber (KF) by melt mixing technique. The mechanical and dynamic mechanical properties, morphology and crystallization behavior were investigated for PBS/KF composites with different KF contents (0, 10, 20, and 30 wt %). The tensile modulus, storage modulus and the crystallization rate of PBS in the composites were all efficiently enhanced. With the incorporation of 30% KF, the tensile modulus and storage modulus (at 40°C) of the PBS/KF composite were increased by 53 and 154%, respectively, the crystallization temperature in cooling process at 10°C/min from the melt was increased from 76.3 to 87.7°C, and the half‐time of PBS/KF composite in isothermal crystallization at 96 and 100°C were reduced to 10.8% and 14.3% of that of the neat PBS, respectively. SEM analysis indicates that the adhesion between PBS and KF needs further improvement. These results signify that KF is efficient in improving the tensile modulus, storage modulus and the crystallization rate of PBS. Hence, this study provides a good option for preparing economical biodegradable composite. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Investigation of mechanical properties of alumina nanoparticle‐loaded hybrid glass/carbon‐fiber‐reinforced epoxy composites

This research work investigates the tensile strength and elastic modulus of the alumina nanoparticles, glass fiber, and carbon fiber reinforced epoxy composites. The first type composites were made by adding 1–5 wt % (in the interval of 1%) of alumina to the epoxy matrix, whereas the second and third categories of composites were made by adding 1–5 wt % short glass, carbon fibers to the matrix. A fourth type of composite has also been synthesized by incorporating both alumina particles (2 wt %) and fibers to the epoxy. Results showed that the longitudinal modulus has significantly improved because of the filler additions. Both tensile strength and modulus are further better for hybrid composites consisting both alumina particles and glass fibers or carbon fibers. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 39749.     

A comparative analysis of woven jute/glass hybrid polymer composite with and without reinforcing of fly ash particles

The objective of this research article is to compare the mechanical and tribological properties of jute‐glass‐fiber‐reinforced epoxy (J‐G‐E) hybrid composites with and without fly ash particulate filler. A dry hand lay‐up technique is used to fabricate all the laminates. The properties including flexural strength, tensile strength, flexural modulus, and erosion behavior of all the composites are evaluated as per American Society for Testing and Materials (ASTM) standards. The fly ash particulate‐filled hybrid composite shows a better mechanical and tribological property. The maximum flexural strength and flexural modulus are obtained for GJGJ+ 5 wt% fly ash filler epoxy composites. Whereas the maximum tensile strength is obtained for GJJG+ 10 wt% fly ash filler epoxy composites. Scanning Electron Microscopy (SEM) analysis also has been carried out to categorize mechanical and tribological behavior of composites. POLYM. COMPOS. 37:658–665, 2016. © 2014 Society of Plastics Engineers     

Development of Silicon Carbide Reinforced Jute Epoxy Composites: Physical,Mechanical and Thermo-mechanical Characterizations

The aim of the present study was to investigate the physical and thermo-mechanical characterization of silicon carbide filled needle punch nonwoven jute fiber reinforced epoxy composites. The composite materials were prepared by mixing different weight percentages (0–15 wt.%) of silicon carbide in needle punch nonwoven jute fiber reinforced epoxy composites by hand-lay-up techniques. The physical and mechanical tests have been performed to find the void content, water absorption, hardness, tensile strength, impact strength, fracture toughness and thermo-mechanical properties of the silicon carbide filled jute epoxy composites. The results indicated that increase in silicon carbide filler from 0 to 15 wt.% in the jute epoxy composites increased the void content by 1.49 %, water absorption by 1.83 %, hardness by 39.47 %, tensile strength by 52.5 %, flexural strength by 48.5 %, and impact strength by 14.5 % but on the other hand, decreased the thermal conductivity by 11.62 %. The result also indicated that jute epoxy composites reinforced with 15 wt.% silicon carbide particulate filler presented the highest storage modulus and loss modulus as compared with the unfilled jute epoxy composite.     

Epoxy composites based on inexpensive char filler obtained from plastic waste and natural resources

In this study, plastic [polyethylene terephthalate (PET)] waste was recycled as raw material for the preparation of diglycidyl ether of bisphenol A‐type epoxy composite materials. The other inexpensive fillers used to prepare the composites were wood shavings char and pine cone char (PCC), obtained from natural resources. The thermogravimetric analysis showed that plastic waste char (PWC) and PCC can significantly improve the thermal stability of neat epoxy resin at temperatures above 300°C. The best thermal and electrical conductivity results were obtained with PWC. The residual weight of the composite with 30 wt% PWC was 69%. Surface hardness, Young's modulus, and tensile strength of the composites were higher than those with a pure epoxy polymer matrix. The composite morphology was characterized by X‐ray diffraction and scanning electron microscopy. POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Preparation,morphology, and properties of silane‐modified MWCNT/epoxy composites

Both epoxy resin and acid‐modified multiwall carbon nanotube (MWCNT) were treated with 3‐isocyanatopropyltriethoxysilane (IPTES). Scanning electron microscopy (SEM) and transmission electronic microscope (TEM) images of the MWCNT/epoxy composites have been investigated. Tensile strength of cured silane‐modified MWCNT (1.0 wt %)/epoxy composites increased 41% comparing to the neat epoxy. Young's modulus of cured silane‐modified MWCNT (0.8 wt %)/epoxy composites increased 52%. Flexural strength of cured silane‐modified MWCNT (1.0 wt %)/epoxy composites increased 145% comparing to neat epoxy. Flexural modulus of cured silane‐modified MWCNT (0.8 wt %)/epoxy composites increased 31%. Surface and volume electrical resistance of MWCNT/epoxy composites were decreased with IPTES‐MWCNT content by 2 orders and 6 orders of magnitude, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Utilization of polyethylene terephthalate waste as a carbon filler in polypropylene matrix: Investigation of mechanical,rheological, and thermal properties

Polyethylene terephthalate (PET) waste was converted into carbon and the feasibility of utilizing it as a reinforcing filler material in a polypropylene (PP) matrix was investigated. The carbon produced by the pyrolysis of waste PET at 900°C in nitrogen atmosphere contains high carbon content (>70 wt%). PP/carbon composites were produced by melt blending process at varying loading concentrations. Scanning electron microscopy images at the fractured surface revealed that the carbon filler has better compatibility with the PP matrix. The mechanical, thermal, and rheological properties and surface morphology of the prepared composites were studied. The thermogravimetric analysis studies showed that the thermal stability of the PP/carbon composites was enhanced from 300 to 370°C with 20 wt% of carbon. At lower angular frequency (0.01 rad/s), the storage modulus (G′) of PP was 0.27 Pa and those of PP with 10 and 20 wt% carbon was 4.06 and 7.25 Pa, respectively. Among the PP/carbon composite prepared, PP with 5 wt% carbon showed the highest tensile strength of 38 MPa, greater than that of neat PP (35 MPa). The tensile modulus was enhanced from 0.9 to 1.2 GPa when the carbon content was increased from 0 to 20 wt%.     

Influence of silicon carbide filler on mechanical and dielectric properties of glass fabric reinforced epoxy composites

Fiber‐reinforced polymeric composites (FRPCs) have emerged as an important material for automotive, aerospace, and other engineering applications because of their light weight, design flexibility, ease of manufacturing, and improved mechanical performance. In this study, glass‐epoxy (G‐E) and silicon carbide filled glass‐epoxy (SiC‐G‐E) composite systems have been fabricated using hand lay‐up technique. The mechanical properties such as tensile strength, tensile modulus, elongation at break, flexural strength, and hardness have been investigated in accordance with ASTM standards. From the experimental investigations, it has been found that the tensile strength, flexural strength, and hardness of the glass reinforced epoxy composite increased with the inclusion of SiC filler. The results of the SiC (5 wt %)‐G‐E composite showed higher mechanical properties compared to G‐E system. The dielectric properties such as dielectric constant (permittivity), tan delta, dielectric loss, and AC conductivity of these composites have been evaluated. A drastic reduction in dielectric constant after incorporation of conducting SiC filler into epoxy composite has been observed. Scanning electron microscopy (SEM) photomicrographs of the fractured samples revealed various aspects of the fractured surfaces. The failure modes of the tensile fractured surfaces have also been reported. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Corundum Fillers with Variable Sizes and Shapes for Epoxy Nanocomposites as High‐Performance Chemical Anchoring and Bonding Systems

Herein, the influence of corundum filler types and contents on the morphological, thermal, and mechanical properties of epoxy nanocomposites tailored for applications as chemical anchoring and bonding systems is investigated. Up to 65 wt% corundum particles with aspect ratios (AR) varying between 1 and 70, average particle sizes ranging from 500 nm to 48 µm, and nanoplatelet thickness varying from 40 to 300 nm, are uniformly dispersed in amine‐cured epoxy resins. At both 25 and 50 wt% filler content, the properties of corundum/epoxy composites are far superior to those of the corresponding benchmark epoxy composites containing a conventional filler such as cement, talcum, or sand. The incorporation of corundum nanoplatelets with AR of 50, length of 2 µm, and thickness of 40 nm, significantly improves Young's modulus (3.5–9.8 GPa) and fracture toughness K_Ic (0.83–1.24 MPa of epoxy nanocomposites at the expense of tensile strength (72–49 MPa). The pull‐out values of the corresponding chemical anchoring systems substantially improve with decreasing sub‐micrometer corundum particle sizes and correlate with tensile strength of the corundum/epoxy nanocomposites, but are much less dependent on corundum particle morphologies, filler aspect ratio, and Young's modulus of the corundum/epoxy composite.     

Epoxy composites based on amino‐silylated MMT: The role of interfaces and clay morphology

Epoxy‐based composites containing sodium montmorillonite (MMT) modified by silylation reaction with 3‐aminopropyltriethoxysilane (A1100) and N‐(2‐aminoethyl)‐3‐aminopropyltrimethoxysilane (A1120) were prepared. The effect of MMT chemical functionalization, as well as inorganic content and dispersion method (i.e., sonication or combination of sonication and ball‐milling) on the morphology and mechanical and thermal properties of composites was thoroughly investigated by X‐ray diffraction analysis, dynamic mechanical and tensile static analysis, nanoindentation measurements and cone calorimeter tests. Morphological characterization showed that the MMT particles are only slightly intercalated by epoxy molecules. Tensile stress, elongation at failure, and toughness of the epoxy composites based on silylated MMT were found to be improved. The presence of 1 and 3% wt/wt of A1100 and A1120 silylated MMT clays allowed the tensile elastic modulus to increase respectively, of about 10 and 15% with respect to the pristine epoxy matrix. The overall results showed that (1) the silylation of MMT clays is a valuable method to improve the interfacial interaction between filler and epoxy matrix and (2) the interfacial interaction plays a role more significant than the clay morphology (i.e., the extent of clay intercalation/exfoliation) over the composite properties. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012