Tensile and impact properties of carbon filled nylon‐6,6 based resins

Electrically and thermally conductive resins can be produced by adding conductive fillers to insulating polymers. Mechanical properties such as tensile modulus, ultimate tensile stress, strain at ultimate tensile stress, and notched Izod impact strength are also important and cannot be ignored. This study focused on performing compounding runs, followed by injection molding and evaluation of tensile and impact properties of carbon filled nylon‐6,6 based resins. The three carbon fillers investigated include an electrically conductive carbon black, synthetic graphite particles, and a surface treated polyacrylonitrile (PAN) based carbon fiber. Resins containing varying amounts of these single carbon fillers were produced and tested. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate. The addition of carbon fiber increased the composite tensile modulus, ultimate tensile stress, and impact strength. Also, in many cases, combining two or three different fillers caused a statistically significant effect at a 95% confidence level. When comparing the results of this study with prior work, it appears that increased heteroatoms present on the carbon fiber surface likely improve composite ultimate tensile stress and impact strength. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2881–2893, 2004     

Tensile properties of carbon filled liquid crystal polymer composites

Electrically and thermally conductive resins can be produced by adding carbon fillers. Mechanical properties such as tensile modulus, ultimate tensile strength, and strain at ultimate tensile strength are vital to the composite performance in fuel cell bipolar plate applications. This research focused on performing compounding runs followed by injection molding and tensile testing of carbon filled Vectra A950RX liquid crystal polymer composites. The four carbon fillers investigated included an electrically conductive carbon black, thermocarb synthetic graphite particles, and two carbon fibers (Fortafil 243 and Panex 30). For each different filler type, resins were produced and tested that contained varying amounts of these single carbon fillers. The carbon fiber samples exhibited superior tensile properties, with a large increase in tensile modulus over the base polymer, and very low drop in the ultimate tensile strength as the filler volume fraction was increased. The strain at the ultimate tensile strength was least affected by the addition of the Panex carbon fiber but was significantly affected by the Fortafil carbon fiber. In general, composites containing synthetic graphite did not perform as well as carbon fiber composites. Carbon black composites exhibited poor tensile properties. POLYM. COMPOS., 29:15–21, 2008. © 2007 Society of Plastics Engineers     

Tensile modulus modeling of carbon‐filled nylon 6,6 and polycarbonate‐based resins

Electrically and thermally conductive resins can be produced by adding conductive fillers to insulating polymers. Mechanical properties, such as tensile modulus, are also important. This research focused on performing compounding runs followed by injection molding and tensile testing of carbon‐filled nylon 6,6 and polycarbonate‐based resins. The three carbon fillers investigated included an electrically conductive carbon black, synthetic graphite particles, and a milled pitch–based carbon fiber. For each polymer, resins were produced and tested that contained varying amounts of these single‐carbon fillers. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate in each polymer. These tensile modulus experimental results were then compared to results predicted by several different models. For the composites containing only one filler type, the Nielsen model with the modified Ψ term provided the best prediction of the actual experimental values. For the composites containing more than one filler type, a new parameter, which includes the vibrated bulk density (VBD) of the fillers, was incorporated into the Nielsen model with the modified Ψ term. This model with the new VBD parameter provided the best estimate of experimental tensile modulus for composites containing multiple‐filler types. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1716–1728, 2003     

Synergistic effects of carbon fillers on tensile and flexural properties in liquid‐crystal polymer based resins

One emerging market for thermally and electrically conductive resins is bipolar plates for use in fuel cells. Adding carbon fillers to thermoplastic resins increases the composite thermal and electrical conductivity. These fillers have an effect on the composite tensile and flexural properties, which are also important for bipolar plates. In this study, various amounts of three different types of carbon (carbon black, synthetic graphite particles, and carbon fibers) were added to Vectra A950RX liquid‐crystal polymer. In addition, composites containing combinations of fillers were also investigated via a factorial design. The tensile and flexural properties of the resulting composites were then measured. The objective of this study was to determine the effects and interactions of each filler with respect to the tensile and flexural properties. The addition of carbon black caused the tensile and flexural properties to decrease. Adding synthetic graphite particles caused the tensile and flexural modulus to increase. The addition of carbon fiber caused the tensile and flexural modulus and ultimate flexural strength to increase. In many cases, combining two different fillers caused a statistically significant effect on composite tensile and flexural properties at the 95% confidence level. For example, when 40 wt % synthetic graphite particles and 4 wt % carbon black were combined, the composite ultimate tensile and flexural strength increased more than what would be expected from the individual additive effect of each single filler. It is possible that linkages were formed between the carbon black and synthetic graphite particles that resulted in improved ultimate tensile and flexural strength. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Thermally conductive nylon 6,6 and polycarbonate based resins. I. Synergistic effects of carbon fillers

Increasing the thermal conductivity of typically insulating polymers, such as nylon 6,6, opens new markets. A thermally conductive resin can be used for heat‐sink applications. This research focused on performing compounding runs followed by injection molding and thermal conductivity testing of carbon filled nylon 6,6 and polycarbonate based resins. The three carbon fillers investigated included an electrically conductive carbon black, synthetic graphite particles, and a milled pitch‐based carbon fiber. For each polymer, conductive resins were produced and tested that contained varying amounts of these single carbon fillers. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate in each polymer. The objective of this article was to determine the effects and interactions of each filler on the thermal conductivity properties of the conductive resins. From the through‐plane thermal conductivity results, it was determined that for both nylon 6,6 and polycarbonate based resins, synthetic graphite particles caused the largest increase in composite thermal conductivity, followed by carbon fibers. The combination of synthetic graphite particles and carbon fiber had the third most important effect on composite thermal conductivity. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 112–122, 2003     

Shielding effectiveness of carbon-filled nylon 6,6

Electrically conductive resins can be made by adding electrically conductive fillers to typically insulating polymers. Resins with an electrical resistivity of approximately 10⁰ ohm-cm or less can be used for electromagnetic and radio frequency interference shielding applications. This research focused on performing compounding runs followed by injection molding and shielding effectiveness testing of carbon filled nylon 6,6 based resins. The three carbon fillers investigated included an electrically conductive carbon black, synthetic graphite particles, and a surface-treated polyacrylonitrile (PAN)-based carbon fiber. Conductive resins were produced and tested that contained varying amounts of these single carbon fillers. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate. The objective of this paper was to determine the effects and interactions of each filler on the shielding effectiveness properties of the conductive resins. Carbon fiber caused the largest increase in shielding effectiveness. Also, all the single fillers and combinations of fillers were statistically significant at the 95% confidence level, except the composite containing carbon black and synthetic graphite particles tested at 800 MHz. Polym. Compos. 25:407–416, 2004. © 2004 Society of Plastics Engineers.     

Thermally conductive nylon 6,6 and polycarbonate based resins. II. Modeling

Increasing the thermal conductivity of typically insulating polymers opens new markets. A thermally conductive resin can be used for heat‐sink applications. This research focused on extruding followed by injection molding and thermal conductivity testing of carbon filled nylon 6,6 and polycarbonate‐based resins. The three carbon fillers investigated included an electrically conductive carbon black, synthetic graphite particles, and a milled pitch‐based carbon fiber. For each polymer, conductive resins were produced and tested that contained varying amounts of these single carbon fillers. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate in each polymer. These through‐plane thermal conductivity experimental results were then compared to results predicted by several different thermal conductivity models. An improved thermal conductivity model was developed that fit the experimental results well for resins that contained single fillers and combinations of different fillers. This improved model was based on the original Nielsen model. A single value for the shape parameter, A (which is needed in Nielsen's model), was used for all three different fillers. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 123–130, 2003     

Thermally conductive carbon filled nylon 6,6

Increasing the thermal conductivity of typically insulating polymers, such as nylon 6,6, opens new markets. A thermally conductive resin can be used for heat sink applications. This research focused on performing compounding runs followed by injection molding and through-plane thermal conductivity testing of carbon filled nylon 6,6 based resins. The three carbon fillers investigated included an electrically conductive carbon black, synthetic graphite particles, and a surface treated polyacrylonitrile (PAN) based carbon fiber. Conductive resins were produced and tested that contained varying amounts of these single carbon fillers. In addition, combinations of fillers were investigated by conducting a full 2³ factorial design and a complete replicate. The objective of this paper was to determine the effects and interactions of each filler on the thermal conductivity of the resins. Synthetic graphite particles caused the largest increase in composite thermal conductivity. In addition, all the single fillers and combinations of fillers caused a statistically significant (at the 95% confidence level) increase in composite thermal conductivity. Polym. Compos. 25:186–193, 2004. © 2004 Society of Plastics Engineers.     

Effects of carbon fillers on tensile and flexural properties in polypropylene‐based resins

A potential application for conductive resins is in bipolar plates for use in fuel cells. The addition of carbon filler can increase the electrical and thermal conductivities of the polymer matrix but will also have an effect on the tensile and flexural properties, important for bipolar plates. In this research, three different types of carbon (carbon black, synthetic graphite, and carbon nanotubes) were added to polypropylene and the effects of these single fillers on the flexural and tensile properties were measured. All three carbon fillers caused an increase in the tensile and flexural modulus of the composite. The ultimate tensile and flexural strengths decreased with the addition of carbon black and synthetic graphite, but increased for carbon nanotubes/polypropylene composites due to the difference in the aspect ratio of this filler compared to carbon black and synthetic graphite. Finally, it was found that the Nielsen model gave the best prediction of the tensile modulus for the polypropylene based composites. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Tensile modulus modeling of carbon‐filled liquid crystal polymer composites

Electrically and thermally conductive resins can be produced by adding conductive fillers to insulating polymers. Mechanical properties, such as tensile modulus, are also important. This research focused on performing compounding runs followed by injection molding and tensile testing of carbon‐filled Vectra liquid crystal polymer. The two carbon fillers investigated were Thermocarb synthetic graphite particles and Fortafil carbon fiber at varying filler amounts. The tensile modulus experimental results were compared to results predicted by several different models. It was found that the Halpin Tsai 2D Randomly Oriented fiber model provided the best fit to the experimental data. The degree of filler‐polymer adhesion was also studied with nanoscratch tests for synthetic graphite and carbon fiber fillers in three polymers: Vectra, nylon 6,6, and polycarbonate. The adhesion trends seen in the nanoscratch tests showed qualitative agreement with the tensile modulus, and should be considered in formulating advanced tensile modulus models. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Factorial design approach applied to electrically and thermally conductive nylon 6,6

Increasing the thermal and electrical conductivity of typically insulating polymers, such as nylon 6,6, opens new markets. A thermally conductive resin can be used for heat sink applications. An electrically conductive resin can be used in static dissipative and Electromagnetic Interference/Radio Frequency Interference shielding applications. This research focused on performing compounding runs followed by injection molding and testing (tensile properties, volumetric electrical resistivity, and through‐plane thermal conductivity) of carbon filled nylon 6,6. The four carbon fillers investigated included a PAN‐based carbon fiber (milled, 200μ long), an electrically conductive carbon black, vapor grown graphitic nanotubes, and Thermocarb (high quality synthetic milled graphite). Formulations were produced and tested that contained varying amounts of a single carbon filler. Combinations of fillers were also investigated via conducting half of a 2⁴ factorial design. It was determined that Thermocarb has the largest effect on the thermal conductivity. Increasing Thermocarb increases thermal conductivity. For conductive resins containing only a single filler type, nanotubes caused the electrical resistivity (ER) to decrease the most. For the half fraction factorial design formulations that contain at least one filler type at the higher level, the ER of the conductive resin ranged from 0.1 to 0.3 ohm‐cm.     

Design and fabrication of conductive composite films with high elasticity and strength using hybrid polymer matrix

ABSTRACT

Flexible conductive polymer composites with good mechanical property play an important role in the modern electronic industry. In this study, aromatic poly(amide-imide) (PAI) and thermoplastic polyurethane (TPU), functionalized multi-wall carbon nanotube (FMWCNT) and reduced graphene oxide (RGO), were, respectively, used as polymer matrix and conductive filler to fabricate conductive polymer composites. Combing the advantages of PAI (high strength) and TPU (good elasticity), PAI-TPU/FMWCNT-RGO polymer composites exhibited a high tensile strength of 58.8 MPa and good elongation at break of 255%. On the other hand, the hybrid conductive filler of FMWCNT-RGO possessed a 3D structure, which is beneficial for improving conductive property, and thus a relative high conductivity of 35.9 S m^?1 was achieved. The enhanced mechanical and conductive properties are mainly ascribed from the good compatibility between the polymer matrix and conductive fillers, which promotes the good dispersion of conductive filler into the polymer matrixes.     

Synergistic effect of carbon fillers in electrically conductive nylon 6,6 and polycarbonate based resins

The electrical conductivity of polymeric materials can be increased by the addition of carbon fillers, such as carbon fibers, carbon black, and synthetic graphite. The resulting composites could be used in applications such as electromagnetic and radio frequency interference shielding and electrostatic dissipation. A significant amount of work has been conducted varying the amount of single conductive fillers in a composite material. In contrast, very limited work has been conducted concerning the effect of combinations of various types of conductive fillers. In this study, three different carbon fillers were used: carbon black, synthetic graphite pareticles, and pitch based carbon fiber. Two different polymers were used: nylon 6,6 and polycarbonate. The goal of this project was to determine the effect of each filler and combinations of different fillers on the electrical conductivity of conductive resins. A 2³ factorial design was analyzed to determine the effects of the three different carbon fillers in nylon 6,6 and polycarbonate. The results showed that carbon black caused the largest increase in composite electrical conductivity. The factorial design analysis also showed that combinations of different carbon fillers do have a positive synergistic effect, thereby increasing the composite electrical conductivity.     

Electrical conductivity model evaluation of carbon fiber filled liquid crystal polymer composites

Electrically conductive resins may have applications as fuel cell bipolar plates. The current trend in this technology is a thermosetting polymer as the matrix containing high concentrations of various types of fillers. These fillers are carbon based and electrically conductive powders, particles, or fibers. In this study, we utilized two composite formulations of polyacrylonitrile fibers (Fortafil 243 and Panex 30) in a liquid crystal polymer (Vectra A950RX) with increasing concentrations. Electrical conductivity tests were performed and modified Mamunya and additive models were applied to the experimental data. These models fit the entire range of data for each composite tested. Four alternate models were also produced: linear, quadratic, exponential, and geometric, with a restricted range of electrical conductivity data greater than 10^?2 S/cm. The exponential and the geometric resulted in the best fits over this restricted data range. These particular models may allow researchers to extrapolate beyond the maximum filler concentrations studied here. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Effects of carbon fillers on the rheology of highly filled liquid‐crystal polymer based resins

Adding conductive carbon fillers to insulating resins increases the composite electrical and thermal conductivity. Often, enough of a single type of carbon filler is added to achieve the desired conductivity while still allowing the material to be molded into a bipolar plate for a fuel cell. In this study, various amounts of three different carbons (carbon black, synthetic graphite particles, and carbon fiber) were added to Vectra A950RX liquid‐crystal polymer. The rheological properties of the resulting single‐filler composites were measured. In addition, the rheological properties of composites containing combinations of different carbon fillers were studied via a factorial design. In all cases, the viscosity increased with increasing filler volume fraction and followed a shear‐thinning power‐law model. The factorial design results indicated that each of the single fillers and all the filler combinations caused a statistically significant increase in the composite viscosity when compared at a shear rate of 500 s^?1 or at a stress of 10⁵ Pa. For composites containing synthetic graphite particles and/or carbon fiber, the viscosity variation with the volume fraction of carbon followed a modified Maron–Pierce equation. When compared at a constant volume fraction of carbon, composites containing carbon black showed viscosity enhancement above and beyond that shown by the other composites. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Mechanical and morphological properties of lyocell blends: Comparison with lyocell nanocomposites (I)

The mechanical properties and morphologies of polyblends of lyocell with three different fillers are compared. Poly(vinyl alcohol) (PVA), poly(vinyl alcohol‐co‐ethylene) (EVOH), and poly(acrylic acid‐co‐maleic acid) (PAM) were used as fillers in blends with lyocell produced through solution blending. The variations of their properties with polymer matrix filler content are discussed. The ultimate tensile strength of the PVA/lyocell blend is highest for a blend lyocell content of 30 wt %, and decreases as the lyocell content is increased up to 40 wt %. The ultimate tensile strengths of the EVOH/lyocell and PAM/lyocell blends are highest for a lyocell loading of 20 wt %, and decrease with the increasing filler content. The variations in the initial moduli of the blends with filler content are similar. Of the three blend systems, the blends with PVA exhibit the best tensile properties. Lyocell/organoclay hybrid films were prepared by the solution intercalation method, using dodecyltriphenylphosphonium–Mica (C₁₂PPh‐ Mica) as the organoclay. The variation of the mechanical tensile properties of the hybrids with the matrix polymer organoclay content was examined. These properties were found to be optimal for an organoclay content of up to 5 wt %. Even polymers with low organoclay contents exhibited better mechanical properties than pure lyocell. The addition of organoclay to lyocell to produce nanocomposite films was found to be less effective in improving its ultimate tensile strength than blending lyocell with the polymers. However, the initial moduli of the nanocomposites were found to be higher than those of the polyblend films. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Effects of carbon fillers on the thermal conductivity of highly filled liquid‐crystal polymer based resins

The thermal conductivity of insulating polymers can be increased by the addition of conductive fillers. One potential market for these thermally conductive resins is for fuel cell bipolar plates. In this study, various amounts of three different carbon fillers (carbon black, synthetic graphite particles, and carbon fiber) were added to Vectra A950RX liquid crystal polymer. Because the resulting composites were anisotropic, they were tested for both through‐plane and in‐plane thermal conductivities. The effects of single fillers and combinations of the different fillers were studied via a factorial design. Each single filler caused a statistically significant increase in composite through‐plane and in‐plane thermal conductivities at the 95% confidence level, with synthetic graphite causing the largest increase. All of the composites containing combinations of the different fillers caused statistically significant increases in the composite through‐plane and in‐plane thermal conductivities. It is possible that thermally conductive pathways were formed that linked these carbon fillers, which resulted in increased composite thermal conductivity. Composites containing 70, 75, and 80 wt % synthetic graphite and the composite containing all three fillers (2.5 wt % carbon black, 65 wt % synthetic graphite, and 5 wt % carbon fiber) had in‐plane thermal conductivities of 20 W m^?1 K^?1 or higher, which is desirable for bipolar plates. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Electrically conductive and super-tough polyamide-based nanocomposites

Polymer nanocomposites can exhibit superior multi-functional properties if they possess phase separated morphology at the nanoscale. Despite the huge potential of these materials, there are several fundamental issues including the ultimate microstructures, which need to be resolved to tailor different physical and mechanical properties required for specific applications. A ‘ternary nanocomposites’ approach is adopted to prepare electrically conductive and super-tough¹ (in terms of notched impact energy) hybrid polymer nanocomposites (polyamide 6/carbon nanotube/elastomer) that possess better properties than either of the constituent binary polymer nanocomposites (polyamide 6/carbon nanotubes and polyamide 6/elastomer). The individual roles of the nano-fillers involved in achieving multi-functionality are emphasized. The level of property enhancements of ternary nanocomposites depends essentially on the microstructure inducing a volume exclusion effect and the capability of fillers to activate the plastic deformation mechanisms in the matrix.     

Melt spinning of conducting polymeric composites containing carbonaceous fillers

Fibers produced by melt spinning of conductive polymer composites are attractive for several applications; the main drawback is however reduced processability at high filler concentrations. Carbon nanotubes (CNTs) are considered suitable fillers for conductive polymer composites, replacing conductive grades of carbon black (CB). In this study, the fiber‐forming properties of conductive polymer composites based on a conductive grade of CB and two masterbatches with CNT in a polyethylene matrix were investigated. The CB was also used in a polypropylene matrix for comparison. The rheological properties of the filler‐containing melts in shear and their extensional behavior were evaluated. A piston‐driven device was used to extrude the molten materials through a capillary; different capillary geometries were tested. Fibers were produced at various draw ratios, and their conductivity was determined. To assess the ultimate extensibility, a modified Rheotens method was used. The results showed that a conductive CB grade can have a lower percolation threshold and higher conductivity than a material with CNT. Conductivity decreased with increasing melt draw ratio for both types of fillers. The spinnability of the materials decreased with increasing concentration of filler material and correlations were found between spinnability and melt elasticity. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Toughening of epoxy resins by hydroxy‐terminated,silicon‐modified polyurethane oligomers

Epoxy resins are among the most versatile engineering structural materials. A wide variety of epoxy resins are commercially available, but most are brittle. Several approaches have been used to improve the toughness of epoxy resins, including the addition of fillers, rubber particles, thermoplastics, and their hybrids, as well as interpenetrating polymer networks (IPNs) of acrylic, polyurethane, and flexibilizers such as polyols. This last approach has not received much attention; none of them have been able to suitably increase resin toughness with out sacrificing tensile properties. Therefore, in an attempt to fill this gap, we experimented with newly synthesized hydroxy‐terminated silicon‐modified polyurethane (SiMPU) oligomers as toughening agents for epoxy resins. SiMPU oligomers were synthesized from dimethyl dichlorosilane, poly(ethylene glycol) (weight‐average molecular weight ～ 200), and toluene 2,4‐diisocyanate and characterized with IR, ¹H‐NMR and ¹³C‐NMR, and gel permeation chromatography. The synthesized SiMPU oligomers, with different concentrations, formed IPNs within the epoxy resins (diglycidyl ether of bisphenol A). The resultant IPN products were cured with diaminodiphenyl sulfone, diaminodiphenyl ether, and a Ciba–Geigy hardener under various curing conditions. Various mechanical properties, including the lap‐shear, peel, and impact strength, were evaluated. The results showed that 15 phr SiMPU led to better impact strength of epoxy resins than the others without the deterioration of the tensile properties. The impact strength increased continuously and reached a maximum value (five times greater than that of the virgin resin) at a critical modifier concentration (20 phr). The critical stress intensity factor reached 3.0 MPa m^1/2 (it was only 0.95 MPa m^1/2 for the virgin resin). © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1497–1506, 2003