Nielsen thermal conductivity model for single filler carbon/polypropylene composites

In this study, three different carbon fillers (Thermocarb TC‐300 synthetic graphite, Ketjenblack EC‐600 JD carbon black, and Hyperion Catalysis International's FIBRIL? carbon nanotubes) were added to a polypropylene matrix to produce single filler composites with filler concentrations of up to 80 wt % synthetic graphite (61.6 vol %), 15 wt % carbon black (8.1 vol %), and 15 wt % carbon nanotubes (7.4 vol %). The through‐plane thermal conductivity for each formulation was measured. For the synthetic graphite, carbon black, and carbon nanotubes composites, the Nielsen model was applied to the experimental through‐plane thermal conductivity data. The Nielsen Model presented in this work showed very good agreement with experimental data. The model parameters were similar to those used in the literature for these fillers in other polymers. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of the talc filler content on the mechanical properties of polypropylene composites

This research examines the effect of a microsize/nanosize talc filler on the physicochemical and mechanical properties of filled polypropylene (108MF10 and 33MBTU from Saudi Basic Industries Corp. and HE125MO grade from Borealis) composite matrices. A range of mechanical properties were measured [tensile properties, bending properties, fracture toughness, notched impact strength (at the ambient temperature and ?20°C), strain at break, and impact strength] along with microhardness testing and thermal stability testing from 40 to 600°C as measured by differential thermal analysis and thermogravimetric analysis. Increasing filler content lead to an increase in the mechanical strength of the composite material with a simultaneous decrease in the fracture toughness. The observed increase in tensile strength ranged from 15 to 25% (the maximum tensile strength at break was found to be 22 MPa). The increase in mechanical strength simultaneously led to a higher brittleness, which was reflected in a decrease in the mean impact strength from the initial 18 kJ/m² (for the virgin polypropylene sample) to 14 kJ/m², that is, a 23% decrease. A similar dependency was also obtained for the samples conditioned at ?20°C (a decrease of 12.5%). With increasing degree of filling of the talc–polypropylene composite matrix, the thermooxidative stability increased; the highest magnitude was obtained for the 20 wt % sample (decomposition temperature = 482°C, cf. 392°C for the virgin polymer). © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Effect of dispersion on rheological and mechanical properties of polypropylene/carbon nanotubes nanocomposites

Polypropylene (PP) nanocomposites filled with the pristine multi‐wall carbon nanotubes (CNTs) and the purified CNTs were prepared by melt blending. The microstructure and linear viscoelastic properties wereinvestigated using rheological and morphological measurements. The results show that the purified CNTs disperse uniformly in the PP matrix. At low frequencies, frequency dependence of modulus weakens clearly with the addition of the CNTs, indicating that the long‐range motion of the polymer chains is restrained by the presence of the CNTs. Percolation networks form when the loading levels achieve up to 3 and 1.5 wt% for the composites with the pristine CNTs (PPCNTs) and the purified CNTs (PPcCNTs), respectively. The linear relaxation modulus increases with increasing loading level. And for composites with loading levels above percolation concentration, the modulus appears to reach a plateau at long time scales due to the formation of percolation network. Tensile strength and impact strength are simultaneously improved with the addition of the CNTs. The better the dispersion of the CNTs, the greater the improvement of the tensile strength and the impact strength. POLYM. ENG. SCI., 2012. © 2012 Society of Plastics Engineers     

Comparative study on electrical properties of copper nanowire/polypropylene and carbon nanotube/polypropylene composites

Nanocomposites using copper nanowires (CuNWs) or carbon nanotubes (CNTs) as fillers with polypropylene (PP) as matrix were prepared by miscible solution mixing and precipitation method. Comparative studies on electrical conductivity and electromagnetic interference shielding properties were reported. On the conductivity curve, a plateau was found for both CuNW/PP composite and CNT/PP composite. The plateaus are located at a different concentration range for each composite type: for CuNW/PP composite, it is between 0.8 and 1.7 vol %, while for CNT/PP composite the plateau occurs in a narrower range between 0.4 and 0.6 vol %. The shielding effectiveness (SE) increases with increased concentration of fillers. CNT/PP composite has higher SE at concentrations less than 2 vol %; the two curves cross near 10 dB at this point and at concentrations higher than 2 vol %, CuNW/PP composite has higher SE. © 2014 American Institute of Chemical Engineers AIChE J, 61: 296–303, 2015     

Effect of ultrasound on the morphology and properties of polypropylene/inorganic filler composites

The effects of ultrasonic irradiation on the rheology, structure, and properties of PP/inorganic filler composites were studied. Scanning electron microscopy showed that ultrasound increased the orientation degrees of acicular fillers to the flow direction. WAXD indicated that ultrasound vibration induced sheet fillers orient with its surface perpendicular to the direction of the ultrasound vibration. The orderly rearrangements of fillers in the polymer melt induced by ultrasound vibration can reduce the steric hindrances in the flow field and increase the flowability of the PP/inorganic filler composites. The effect of ultrasound on reducing the apparent viscosities is very prominent, especially at lower shear rate. Ultrasound has an even more marked effect on reducing the apparent viscosities of composites containing fillers of larger size. With ultrasound vibration, the mechanical properties of the composites are also improved because of the orientation and uniform dispersion of fillers in the matrix. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1553–1560, 2005     

Effect of filler dispersion on polypropylene morphology

The evaluation of filler dispersion in compounding machines is an important part of their design. Calcium carbonate–filled polypropylene (PP) was used as a model compound to study filler dispersion. The evolution of dispersion was followed in a twin‐screw extruder where several types of mixing sections were evaluated. Reverse kneading blocks were found to be very efficient for breakup of agglomerates. Depending on extrusion conditions, agglomeration was observed even after the matrix was melted. To study dispersion in a single‐screw extruder, Maddock and reverse Maddock mixing elements were tried. A quantitative evaluation of the dispersion state allowed a better understanding of nucleation in the PP/CaCO₃ matrix. A significant content of the β‐phase of polypropylene was observed when the agglomerate size was relatively small. The level of shear stress was also important for the formation of the β‐phase of PP. The quantification of dispersion was mainly evaluated from micrographs of samples obtained by reflected light microscopy in conjunction with image analysis. The characterization of β‐spherulites was carried out using polarized light microscopy and scanning electron microscopy. Polym. Eng. Sci. 44:880–890, 2004. © 2004 Society of Plastics Engineers.     

The electrical conductivity of carbon nanotube/carbon black/polypropylene composites prepared through multistage stretching extrusion

We reported the design of a grape-cluster-like conductive network in a polypropylene (PP) matrix, where oriented multi-walled carbon nanotubes (MWCNTs) served as branches and provided charge transport over large distances while grape-like carbon black (CB) aggregates enriched around MWCNTs and linked these conductive tubes through charge transport over small distances. The key for construction of this grape-cluster-like conductive network was the extension and orientation of MWCNTs, which was achieved in this work by multistage stretching extrusion with an assembly of laminating-multiplying elements (LMEs, which divide and recombine polymer melts). The highest efficient grape-cluster-like conductive network was obtained at a CB:MWCNT weight ratio of 6. The experimental results showed that this novel grape-cluster-like conductive network provided a low percolation threshold for PP/CB/MWCNT composites due to the synergistic effect of CB and oriented MWCNTs. When the combined CB and MWCNT content was about 6.9 vol%, the electrical resistivity of PP/CB/MWCNT composites prepared by multistage stretching extrusion with 6 LMEs decreased to only 0.63 Ω cm.     

Polyaniline/polypropylene film composites with high electric conductivity and good mechanical properties

Polyaniline/polypropylene composites were prepared by oxidative polymerization of aniline in biaxially stretched polypropylene microporous films with ammonium persulfate as the oxidant. A continuous permeation/diffusion polymerization process was used in order to incorporate more polyaniline in the composite. The influence of reaction time and temperature and the concentration of monomer and oxidant aqueous solutions on the electric conductivity of the composites was investigated. The composites may exhibit a loose particulate surface morphology and a compact surface with a ring-shaped structure. The content and distribution of polyaniline in the composite and, hence, its electric conductivity and surface properties can be controlled over a wide range. Composites with the combination of high electric conductivity and good mechanical properties can be obtained under proper conditions. The composite films were flexible and strong enough and have electric conductivity as high as 5–6 S/cm. © 1995 John Wiley & Sons, Inc.     

Effect of clinoptilolite filler on the physical and mechanical properties of polypropylene

This study aims to investigate the mechanical and physical properties of polypropylene (PP) filled by natural zeolite. For this purpose, a natural zeolite (at 1–6 wt% filler loadings) with two different particle sizes was used. Two different kinds of silane coupling agents (3‐aminopropyltriethoxysilane, GAPTES and 3‐glycidoxypropyltrimethoxysilane, GPTMS) at three different volume ratios were used to improve the zeolite compatibility with PP and to improve the mechanical properties of composites. Fillers and PP were compounded with a twin screw extruder, and the composites were moulded with injection moulding press. The samples were subjected to mechanical tests (i.e., impact and tensile tests) and physical tests (i.e., hardness, density, and melt flow index, MFI). The physical test results showed that the levels of hardness and density of both unmodified and modified zeolite‐filled PP composites were higher compared with neat PP. The MFI values of composites were decreased by increasing zeolite loading level. Composites including GAPTES modified zeolite showed improved yield strength, impact strength and stiffness compared with composites filled with unmodified zeolite particles. POLYM. COMPOS. 34:1396–1403, 2013. © 2013 Society of Plastics Engineers     

Effect of processing technique on the dispersion of carbon nanotubes within polypropylene carbon nanotube‐composites and its effect on their mechanical properties

Carbon nanotube‐reinforced polymer composites are being investigated as promising new materials having enhanced physical and mechanical properties. With regards to mechanical behavior, the enhancements reported thus far by researchers are lower than the theoretical predictions. One of the key requirements to attaining enhanced behavior is a uniform dispersion of the nanotubes within the polymer matrix. Although solvent mixing has been used extensively, there are concerns that any remaining solvent within the composite may degrade its mechanical properties. In this work, a comparison is carried out between solvent and “solvent‐free” dry mixing for dispersing multiwall carbon nanotubes in polypropylene before further melt mixing by extrusion. Various weight fractions of carbon nanotubes (CNTs) are added to the polymer and their effect on the mechanical properties of the resulting composites is investigated. Enhancements in yield strength, hardness, and Young's modulus when compared with the neat polymer, processed under similar conditions, are observed. Differences in mechanical properties and strain as a function of the processing technique (solvent or dry) are also clearly noted. In addition, different trends of enhancement of mechanical properties for the solvent and dry‐mixed extrudates are observed. Dry mixing produces composites with the highest yield strength, hardness, and modulus at 0.5 wt% CNT, whereas solvent mixing produces the highest mechanical properties at CNT contents of 1 wt%. It is believed that this difference is primarily dependent on the dispersion of CNTs within the polymer matrix which is influenced by the processing technique. Field emission scanning electron microscopy analysis shows the presence of clusters in large wt% CNT samples produced by dry mixing. Samples produced by solvent mixing are found to contain homogeneously distributed CNTs at all CNT wt fractions. CNT pull‐out is observed and may explain the limited enhancement in mechanical properties. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Crystallization behavior and mechanical properties of polypropylene/modified carbon black composites

Carbon black (CB) modified with small organic molecules was filled in polypropylene (PP) matrix. The crystallization behavior and mechanical properties of PP/modified CB (MCB) composites were investigated. Compared with the original CB, MCB could be dispersed uniformly in smaller particle sizes in PP matrix, and MCB could act as a more effective nucleating, toughening, and reinforcing agent when it was filled in PP at low concentrations. Further increasing of MCB particles in PP matrix resulted in the decrease of impact and tensile strength of PP/MCB composites. It was inferred from DSC results that the existence of CB vand MCB in PP matrix could result in the decrease of crystallite size and degree of perfection of PP. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Effect of filler partitioning on the mechanical properties of TPO/nanosilica composites

Nanosilica (SiO₂) is used as a reinforcing filler in PP/elastomer thermoplastic polyolefin (TPO) blends containing ethylene‐octene polyolefin elastomer (POE), ethylene‐propylene rubber (EPR), and maleated EPR. The localization and dispersion of the filler are controlled by adding maleated derivatives to the matrix or the dispersed phase. A separated morphology, consisting of SiO₂ residing in the PP matrix, is necessary to achieve improvements in modulus. Filled TPOs containing POE have the best performance and exhibit improved moduli while retaining high values of elongation. J. VINYL ADDIT. TECHNOL., 13:147–150, 2007. © 2007 Society of Plastics Engineers     

Nylon 6 induced morphological developments and electrical conductivity improvements of polypropylene/carbon black composites

In this study, a polar conductive filler [carbon black (CB)], a nonpolar polymer [polypropylene (PP)], and a polar polymer [nylon 6 (PA6)] were chosen to fabricate electrically conductive polymer composites by melt blending and compression molding. The morphological developments of these composites were studied. Scanning electron microscopy results showed that in a CB‐filled PP/PA6 (CPA) composite, CB particles were selectively dispersed in PA6 phases and could make the dispersed particles exist as microfiber particles, which could greatly improve the electrical conductivity. The PA6 and CB contents both could affect the morphologies of these composites. The results of electrical resistivity measurements of these composites proved the formation of conductive networks. The resistivity–temperature behaviors of these composites were also studied. For CB‐filled PP (CP) composites, there were apparent positive temperature coefficient (PTC) and negative temperature coefficient (NTC) effects and an unrepeatable resistivity–temperature characteristic. However, for CPA composites, there were no PTC or NTC effects from room temperature to 180°C, and the resistivity–temperature behavior showed a repeatable characteristic; this proved that CB particles were selectively dispersed in the PA6 phase from another point of view. All experimental results indicated that the addition of PA6 to a CP composite could lead to an expected morphological structure and improve the electrical conductivity of the CP composite. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Influence of PANI‐complex on the mechanical and electrical properties of carbon fiber reinforced polypropylene composites

The aim of this work was to determine the influence of PANI‐complex on the mechanical and electrical properties of CF‐PP composites. As expected, an increase in tensile strength and modulus of the PP matrix could be achieved with an increasing fiber weight fraction. On the other hand, the PANI‐complex decreased the tensile strength and modulus of the fiber reinforced composites; however, these values remained on a better level than the value of the neat PP. Further, by using a long carbon fiber (LCF) reinforcement instead of short carbon fibers (SCF) the percolation threshold was moved towards a lower fiber weight content. In addition, a synergy effect between PANI‐complex and LCF in the PP‐matrix regarding the electrical properties occurred. In particular, an abrupt decrease in the surface resistivity could be avoided. Also, the surface resistivity of a blend is better when the blend consists of both PANI‐complex and LCF instead of only one of these fillers.     

Syndiotactic polypropylene/microfibrous cellulose composites: Effect of filler size on tensile properties

Syndiotactic polypropylene (SPP)/ethanol swelled microfibrous cellulose (MFC) composite was prepared by a melting mixer, and its morphology and tensile properties were studied. The scanning electron microscope microphotograph did not show the aggregated MFC part up to the 40 wt % MFC loading content, and the Young's modulus was exponentially increasing with the increase of the MFC loading content. These results suggested that the MFC was well‐dispersed in the SPP matrix by an ethanol surfactant work. The Young's modulus was much higher than that of the composite with commonly used fibrous cellulose and moreover, exceeded the theoretical one obtained from the Halpin‐Tsai equation. The differential scanning calorimetry and wide‐angle X‐ray diffraction measurements showed that the MFC acted as a good α‐nucleation agent for SPP. It was found that the excessive Young's modulus of the MFC composite was originated from an increase of that of the SPP matrix induced by the α‐nucleation effect. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Morphology and electrical conductivity of injection-molded polypropylene/carbon black composites with addition of high-density polyethylene

This work attempts to clarify the influence of carbon black (CB) addition on the microstructure of injection-molded high-density polyethylene (HDPE)/polypropylene (PP) blends and effect of shear-induced polymer deformation on the conductive network structure. We observed that HDPE molecules are strongly interacted with carbon surfaces and CB particles are selectively located in HDPE domains. Morphology of the injection-molded specimen consists of three parts, namely, CB-HDPE complex domain, free HDPE domain and PP domain. The volume and microstructure of the free HDPE domain are significantly influenced by HDPE and CB concentration, CB structure, and PP viscosity. We also confirmed that the CB particles are capable of self-assembly to form random conductive networks even under high shear rate within very short time. The morphological changes were finally correlated to the variation of electrical conductivity.     

Effect of corona modification on the mechanical properties of polypropylene/cellulose composites

The effect of various corona treatment conditions on the mechanical properties of cellulose fibers/polypropylene composites was studied. The cellulose fibers and polypropylene were modified using a wide range of corona treatment levels and concentrations of oxygen. The treatment level of the fibers was evaluated using the electrical conductance of their aqueous suspensions. The mechanical properties of composites obtained from different combinations of treated or untreated cellulose fibers and polypropylene were characterized by tensile stress–strain measurements; they improved substantially when either the cellulose fibers alone or both components were treated, although composites made from untreated cellulose fibers and treated polypropylene showed a relatively small improvement. The results obtained indicate that dispersive forces are mostly responsible for the enhanced adhesion. The relationship between the electrical conductance of the fibers, the mechanical properties, and the mechanism of improved adhesion is discussed. © 1994 John Wiley & Sons, Inc.     

The effect of filler content and size on the mechanical properties of polypropylene/oil palm wood flour composites

The effect of filler content and size on the mechanical properties of a new type of wood-based filler, oil palm wood flour (OPWF), in polypropylene (PP) was investigated. Four sizes of OPWF filler at different filler loadings were compounded using a twin screw compounder. All sizes of filler showed a similar trend of declining mechanical properties with increasing filler content. In terms of size, the composites filled with larger-sized filler showed higher modulus, tensile and impact strengths, particularly at high filler loadings. The OPWF used in this study was not treated with any coupling agent.     

Effect of carbon nanotube length on thermal,electrical and mechanical properties of CNT/bismaleimide composites

Multi-wall carbon nanotubes (MWCNTs) with lengths of 0.65–1.3 mm were used to fabricate aligned and continuous MWCNT/bismaleimide composites. We found that longer CNTs resulted in higher thermal and electrical conductivities of the composites. The tensile strength and Young’s modulus, however, exhibited no CNT length dependency. Investigation of the CNT morphology by transmission electron microscopy revealed that the average nanotube diameter and wall number also increased with the CNT length, while the aspect ratio remained nearly unchanged. The structural changes significantly affected the phonon and electron transport in the composite structure, but the interplay of increased CNT length and diameter led to no appreciable change in the mechanical properties of the composites.     

Kinetics of filler wetting and dispersion in carbon nanotube/rubber composites

The effects of the surface modification of multi-walled carbon nanotubes (MWCNTs) by an ionic liquid, 1-butyl 3-methyl imidazolium bis(trifluoromethyl-sulphonyl)imide (BMI) on the kinetics of filler wetting and dispersion as well as resulting electrical conductivity of polychloroprene (CR) composites were studied. Two different MWCNTs were used, Baytubes and Nanocyl, which differ in their structure, purity and compatibility to CR and BMI. The results showed that BMI can significantly improve the macrodispersion of Baytubes, and increases the electrical conductivity of the uncured BMI–Baytube/CR composites up to five orders of magnitude. In contrast, the use of BMI slows the dispersion process and the development of conductivity of BMI–Nanocyl/CR composites. Our wetting concept was further developed for the quantification of the bound polymer on the CNT surface. We found that the bonded BMI on the CNT surface is replaced by the CR molecules during mixing as a result of the concentration compensation effect. The de- and re-agglomeration processes of CNTs taking place during the subsequent curing process can increase or decrease the electrical conductivity significantly. The extent of the conductivity changes is strongly determined by the composition of the bound polymer and the curing technique used.