Microstructural and microwave shielding characteristics of water‐soluble polypyrrole–polyvinyl alcohol–graphite oxide core–shell nanocomposites

This article reports on a facile route for the preparation of polypyrrole–polyvinyl alcohol–graphite oxide nanocomposites through the polymerization of pyrrole with different concentration (wt%) of graphite oxide using ammonium persulfate as an oxidant. The synthesized nanocomposites were characterized by Fourier transform infrared spectroscopy, and their surface morphologies were studied by scanning electron microscopy and transmission electron microscopy. Their solubility in water, DC conductivity in solution, and the current–voltage characteristics of the nanocomposites were studied. Furthermore, the microwave absorption at 1.0–10.0 MHz and the effects of sample thickness on the microwave absorption were investigated. The composites including higher concentration of graphite oxide showed increased solubility and electrical conductivity, and high electromagnetic shielding effectiveness. POLYM. COMPOS. 2012. © 2012 Society of Plastics Engineers     

New generation layered nanocomposites derived from ethylene‐co‐vinyl acetate and naturally occurring graphite

New ethylene‐co‐vinyl acetate (EVA, with 60% vinyl acetate content) based nanocomposites were prepared with graphites modified by various techniques and a commercially available expanded graphite (EG). The infrared spectra and the surface energy measurements indicated better oxidation and higher surface energy of the graphite modified by mixed acids followed by high temperature treatment (GO). Interlayer space and surface area were increased as a result. EG possessed higher surface area. GO was found to distribute in finer tactoids of average thickness of 25 nm in the matrix, as compared with the unmodified graphite (UG), having average tactoid thickness more than 40 nm along with aggregation. EG also showed finer dispersion in the EVA matrix with some network formation. The dynamic mechanical and the mechanical properties were superior at the 2 wt % concentration of the GO, beyond which the improvement was less, possibly because of aggregation of GO. Greater EVA‐GO interaction at 2 wt % concentration was also supported from the swelling analysis, thermal conductivity, and the thermo‐oxidative degradation data of the hybrid composites. The melt viscosity was lower at 2 wt % GO concentration. EG based nanocomposites registered similar properties. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

One‐step synthesis of highly conductive PPy/graphite nanosheets/Gd3+ composites

Highly conductive polypyrrole/graphite nanosheets/Gd³⁺ (PPy/nanoG/Gd³⁺) composites are fabricated via in situ polymerization using p‐toluenesulfonic acid as a dopant and FeCl₃ as an oxidant. The effects of the graphite nanosheets and Gd³⁺ loading on the electrical conductivity are investigated. The maximum conductivity of PPy/nanoG/Gd³⁺ composites about 17.86 S/cm found with 3 wt% graphite nanosheets and 6 wt% Gd³⁺ at room temperature. The results showed that the high‐aspect‐ratio structure of graphite nanosheets played an important role in forming a conducting network in PPy matrix. Thermal gravimetric analysis demonstrates an improved thermal stability of PPy in the PPy/nanoG/Gd³⁺ composites. The microstructures of PPy/nanoG/Gd³⁺ are evidenced by the SEM and TEM examinations. POLYM. COMPOS., © 2011 Society of Plastics Engineers.     

Electrically conductive foamed polyurethane/silicone rubber/graphite nanocomposites as radio frequency wave absorbing material: The role of foam structure

Radio frequency wave absorber nanocomposites based on a flexible polyurethane (PU) foam has been manufactured by impregnation of the foam in n‐hexane solution of room temperature vulcanizing silicone rubber (SR), hybridized with graphite nanosheets (GNs) called doping solution. After impregnation, dried samples were kept at ambient temperature for the curing of the soaked graphitized SR. To evaluate the influences of the PU foam structural parameters on electrical conductivity, permittivity, and reflection loss characteristics, various foams with different structures were impregnated in the crosslinkable doping solution. Electrical conductivity, real, and imaginary parts of permittivity were measured within the frequency range of 4–6 GHz via performing waveguide measurements. The coarse thick wall PU foam sample exhibited higher conductivity and permittivity than the fine wire mesh sample having similar amounts of conductive SR/GN doping agent. Moreover, nanocomposites based on coarse foam samples showed higher potential for the wave absorption at lower absorber thickness than the fine wire mesh PU foam. The higher conductivity and hence imaginary permittivity of the coarse structure is attributed to the better coincidence of conductive paths in the PU/SR/GN nanocomposite foam with lines of electric field of the incident wave. The higher real permittivity of the coarse nanocomposite is suggested to be related to the more mutual interactions between graphite nanolayers and aggregates which form a network of minicapacitors in the structure of nanocomposites, leading to a higher capacitance and hence more real permittivity. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Preparation of polystyrene–graphite conducting nanocomposites via intercalation polymerization

In situ polymerization of styrene was conducted in the presence of expanded graphite obtained by rapid heating of a graphite intercalation compound (GIC), to form a polystyrene–expanded graphite conducting composite. The composite showed excellent electrically conducting properties even though the graphite content was much lower than in normal composites. The transition of the composite from an electrical insulator to an electrical semiconductor occurred when the graphite content was 1.8 wt%, which is much lower than that of conventional conducting polymer composites. TEM, SEM and other studies suggest that the graphite was dispersed in the form of nanosheets in a polymer matrix with a thickness of 10–30 nm, without modification of the space between carbon layers and the structure of the graphite crystallites. The composite exhibited high electrical conductivity of 10^?2 S cm^?1 when the graphite content was 2.8–3.0 wt%. This great improvement of conductivity could be attributed to the high aspect ratio (width‐to‐thickness) of the graphite nanosheets. The rolling process strongly affected the conductivity and the mechanical properties of the composite. © 2001 Society of Chemical Industry     

Novel conducting nanocomposite based on polypyrrole and modified poly(styrene‐alt‐maleic anhydride) via emulsion polymerization: Synthesis,Characterization, Antioxidant,and heavy metal sorbent activity

Novel polypyrrole/modified poly(styrene‐alt‐maleic anhydride) conducting nanocomposites were prepared via emulsion polymerization using sodium dodecyl sulfate as an emulsifier and ammonium persulfate as an oxidant. Modified poly(styrene‐alt‐maleic anhydride) was used as an external dopant for conductivity enhancement of polypyrrole. The conductivity of nanocomposites was measured with a four‐probe method. The maximum electrical conductivity of the nanocomposite was 1.40 S/cm. The data from this research showed that the novel nanocomposite presents good tendency for the removal of heavy metal ions from aqueous solutions. Also the prepared nanocomposites were analyzed for their antioxidant activity using 2,2‐diphenyl‐1‐picrylhydrazyl assay. The results showed that the antioxidant activity of the nanocomposite was 60%. The nanocomposites were characterized by Fourier transform infrared, ultraviolet–visible, X‐ray diffraction, field emission scanning electron microscopy, and differential scanning calorimetry measurements. POLYM. COMPOS., 36:138–144, 2015. © 2014 Society of Plastics Engineers     

In situ dynamic vulcanization process in preparation of electrically conductive PP/EPDM thermoplastic vulcanizate/expanded graphite nanocomposites: Effects of state of cure

In situ melt dynamic vulcanization process has been employed to prepare electrically conductive polypropylene (PP)/ethylene–propylene–diene rubber (EPDM) (40/60 wt %) thermoplastic vulcanizates (TPVs) incorporated by expanded graphite (EG) as a conductive filler. Maleic anhydride grafted PP (PP‐g‐MAH) was used as compatibilizer and a sulfur curing system was designed and incorporated to vulcanize the EPDM phase during mixing process. Developed microstructures were characterized using scanning electron microscopy (SEM), melt rheomechanical spectroscopy (RMS), X‐ray diffraction (XRD), and transmission electron microscopy (TEM) and were correlated with electrical conductivity behavior. For comparison, another class of TPV/EG nanocomposites was fabricated using a commercially available PP/EPDM‐based TPV via both direct and masterbatch melt mixing process. Conductivity of the nanocomposites prepared by in situ showed no significant change during dynamic vulcanization till the mixing torque reached to the stationary level where micro‐morphology of the cured rubber droplets was fully developed, and conductivity abrupt was observed. In situ cured nanocomposites showed higher insulator to conductor transition threshold (3.15 vol % EG) than those based on commercially available TPV. All electrically conductive in situ prepared TPV nanocomposites exhibited reinforced melt elasticity with pseudosolid‐like behavior within low frequency region in dynamic melt rheometry indicating formation of physical networks by both EG nanolayers and crosslinked EPDM droplets. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Impact of various oxidation degrees of graphene oxide on the performance of styrene–butadiene rubber nanocomposites

In this work, graphene oxide (GO) with various oxidation degrees were synthesized by adjusting the dosage of oxidation agent based on a modified Hummers' method, and were then used for the fabrication of the styrene–butadiene rubber (SBR)/GO nanocomposites through latex coagulation method, followed by a high‐temperature cure process. The vulcanization characteristics, thermal stability, mechanical properties, thermal conductivity as well as solvent resistance of SBR/GO nanocomposites were investigated. The results indicated that various surface structures of GO due to oxidation degrees may lead to different dispersion states of GO in the rubber matrix, and thus greatly influenced the cure rate, mechanical properties as well as thermal conductivity of SBR/GO nanocomposites. The optimal (moderate) oxidation degree of GO was achieved at the oxidation agent (KMnO₄)/graphite weight ratio 9/5, for which case the tensile strength, tear strength, and thermal conductivity of SBR/GO nanocomposites increased by 271.3%, 112.3%, and 28.6%, respectively, compared with those of neat SBR. In addition, the mentioned nanocomposites also showed the best solvent resistance in toluene. POLYM. ENG. SCI., 58:1409–1418, 2018. © 2017 Society of Plastics Engineers     

Preparation of interfacially compatibilized PP‐EPDM thermoplastic vulcanizate/graphite nanocomposites: Effects of graphite microstructure upon morphology,electrical conductivity,and melt rheology

Electrically conductive PP/EPDM dynamically crosslinked thermoplastic vulcanizate (TPV)/expanded graphite (EG) has been successfully prepared via melt compounding of maleic anhydride grafted polypropylene (PP‐g‐MA)/EG masterbatch and a commercially available TPV material. Correlation between graphite microstructure, and electrical conductivity as well as melt rheological behavior has been studied. Natural graphite flake (NGF), graphite intercalated compound (GIC), and exfoliated graphite (EG) have been employed and compared. Scanning electron microscopy (SEM) showed the presence of 100–200 nm nanolayers in the structure of PP‐g/EG masterbatches, whereas thinner platelets (1.5–2.5 nm) were revealed by transmission electron microscopy (TEM). Better dispersion of the graphite nanolayers in the microstructure of TPV/PP‐g‐MA/EG composite was verified, as the 7.3 Å spacing between the aggregated graphite nanolayers could not be observed in the XRD pattern of this material. TPV/PP‐g/EG nanocomposites exhibited much lower conductivity percolation threshold (φ_c) with increased conductivity to 10^?5 S/cm at EG wt % of 10. Higher nonlinear and nonterminal melt rheological characteristics of dynamic elastic modulus (G′) at low frequency region was presented by the TPV/PP‐g/EG nanocomposites, indicating the formation of nanoscopic conducting multiple networks throughout the continuous TPV matrix. Maleated PP was found to be much more effective in separating EG nanolayers which is attributed to the higher interfacial interaction between PP‐g‐MAH and EG, synergized with its multiporous structure. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Dispersion of graphite nanosheets in a polymer matrix and the conducting property of the nanocomposites

Poly(methyl methacrylate)(PMMA)/expanded graphite composite has been made via an in situ polymerization of methyl methacrylate(MMA) in the presence of expanded graphite obtained by rapid heating of the graphite intercalation compound (GIC). The composite was then blended with poly(vinyl chloride) (PVC) to form an electrically conducting composite. SEM, TEM and XRD showed that the graphite had been dispersed throughout the polymer matrix in the form of nanosheets with thicknesses of about 20 nm. The resulting composite showed excellent electrical conductivity despite a low concentration of graphite. The transition from an electrical insulator to an electrical semiconductor for the composite occurred when the graphite content was 3.5 wt%, much lower than that of conventional conducting polymer composites. Conductivity reached a maximum of 10^?4 s/cm at a graphite concentration of 5.0 wt%. This improvement of conductivity could be attributed to the high aspect ration (width‐to‐thickness) of the graphite nanosheets dispersed in the polymer matrix.     

A study of graphene oxide‐reinforced rubber nanocomposite

Graphene oxide‐reinforced acrylonitrile–butadiene rubber nanocomposites were prepared via solution mixing. The morphology of the graphene oxide was studied, and its successful dispersion within the rubber matrix was confirmed by transmission electron microscopy, scanning electron microscopy, and X‐ray diffraction studies. The strong rubber‐to‐filler interaction was confirmed by swelling and mechanical reinforcing behaviors and thermal stability. Dielectric spectroscopy test indicated a marked improvement of about five times in the real part of permittivity. The electrical conductivity level was close to that of nonconductive materials. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40640.     

Synthesis and properties of poly(4,4′-oxybis(benzene)disulfide)/graphite nanocomposites via in situ ring-opening polymerization of macrocyclic oligomers

An effective method for the preparation of poly(4,4′-oxybis(benzene)disulfide)/graphite nanosheet composites via in situ ring-opening polymerization of macrocyclic oligomers were reported. Completely exfoliated graphite nanosheets were prepared under the microwave irradiation followed by sonication in solution. The nanocomposites were fabricated via in situ melt ring-opening polymerization of macrocyclic oligomers in the presence of graphite nanosheets. The graphite nanosheets and resulted poly(arylene disulfide)/graphite nanocomposites were characterized with field emission scanning electron microscope (FE-SEM), transmission electron microscope (TEM), tensile tester and electrical conductivity measurements. Compared with pure polymer, the electrical conductivity of the poly(arylene disulfide)/graphite nanocomposites were dramatically increased and had a value of about 10⁻³ S/cm for the nanocomposite containing 5 wt% graphite. The nanocomposites exhibit as both high performance polymeric material and electrically conductive material. Therefore, they show potential applications as high temperature conducting materials.     

Thermal,mechanical and morphological properties of surface‐modified montmorillonite‐reinforced Viton rubber nanocomposites

Thermal, mechanical and morphological properties of surface‐modified montmorillonite (OMMT)‐reinforced Viton rubber nanocomposites were studied. The surface of montmorillonite was modified with a column chromatography technique using quaternary long‐chain ammonium salt as an intercalant, which resulted in uniform exchange of ions between montmorillonite and the ion‐exchange resin, and increased the d‐spacing to 31.5 Å. This improved d‐spacing was due to the use of an ion‐exchange column of sufficient length (35 cm) and diameter (5 cm) with maximum retention time for exchange of ions. The Viton nanocomposites reinforced with OMMT (3–12 wt%) were prepared using a two‐roll mill and moulded in a compression moulding machine. Tensile strength increased 3.17 times and elongation at break from 500 to 600% for 9 wt% loading of OMMT in comparison to pristine Viton rubber. Thermogravimetric analysis revealed that the presence of OMMT greatly improved the thermal stability. This improvement in properties with increasing OMMT loading was due to insertion of rubber chains between the OMMT plates with good wetting ability. Overall, at an optimum OMMT loading of 9 wt%, the properties of the Viton rubber nanocomposites improved, and subsequently worsened at 12 wt% due to agglomeration of OMMT as revealed by scanning electron microscopy and atomic force microscopy images. © 2013 Society of Chemical Industry     

Mechanical and functional properties of composites based on graphite and carboxylated acrylonitrile butadiene rubber

In this study, carboxylated acrylonitrile butadiene rubber (xNBR)/expanded graphite (EG) nanocomposites were prepared with a latex compounding technique by ultrasonic stirring. The dispersion of EG in the xNBR matrix was investigated with transmission electron microscopy, scanning electron microscopy, and X‐ray diffraction analysis. EG could be exfoliated into lots of nanosheets dispersing in the xNBR matrix. More EG loading resulted in the presence of a few incompletely exfoliated agglomerates. The mechanical properties (hardness, tensile modulus, and tensile strength) of the xNBR/EG composites were determined. Dynamic mechanical thermal analysis was also performed, and it showed that the nanosheets of EG somewhat immobilized the motion of rubber macromolecular chains and led to the shifting and broadening of the tan δ peak toward higher temperatures. Many other functional properties of EG‐filled xNBR composites were studied, and it was established that the composites had excellent electrical conductivity as well as gas‐barrier and wear properties. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Comparative study on the natural rubber nanocomposites reinforced with carbon black nanoparticles and graphite oxide nanosheets

To achieve dramatic improvements in the performance of natural rubber (NR), the graphite oxide nanosheets (GON)‐reinforced NR nanocomposites have been prepared through solution mixing on the basis of pretreatment of graphite. The mechanical and thermal properties of GON/NR nanocomposites were characterized in contrast to the carbon black (CB)/NR nanocomposite. The mechanical properties of the GON‐reinforced NR showed a considerable increase compared to the neat NR and traditional CB/NR nanocomposite. The initial modulus of pure NR was increased for up to 53.6% when 7 wt% GON is incorporated. The modulus and strength of NR with GON appear to be superior to those of CB with the same filler content. The dispersion state of the nanofillers into NR was investigated by scanning electron microscopy and X‐ray diffraction, and the results indicated that nanofillers have been dispersed homogeneously in the NR matrix. Fourier transform infrared spectra showed possible interfacial interactions between fillers and NR matrix. Differential scanning calorimetry and thermogravimetric analysis showed that the T _g and thermal decomposition temperature of NR slightly increased with the addition of the fillers, especially for that of GON/NR nanocomposites. According to this study, application of the physical and mechanical properties of GON to NR can result in rubber products which have improved mechanical, physical, and thermal properties, compared with existing NR products reinforced with CB. POLYM. COMPOS., 38:1427–1437, 2017. © 2015 Society of Plastics Engineers     

Effects of conductive graphite filler loading on physical properties of high‐density polyethylene composite

High‐density polyethylene (HDPE)/graphite nanocomposites containing up to 30 vol% of graphite powder filler were prepared by melt mixing in a Brabender Plasticorder at 180°C for 15 min. The nanocomposites were characterized for their rheological, dynamic mechanical, crystallographic, and electrical properties as a function of graphite loading. The results indicated that graphite loading affects storage modulus, loss modulus, complex viscosity, and conductivity of HDPE matrix. The storage modulus increases while the graphite loading increases in the studied concentration range (up to 30%). When the graphite loading was increased to 30%, storage modulus at room temperature was about 300% higher than that of pure HDPE. Also, the composites containing 20 and 30% graphite shows more conductivity than the others. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Organoclay‐reinforced dynamically vulcanized thermoplastic elastomers of polyamide‐6/polyepichlorohydrin‐co‐ethylene oxide

Dynamically vulcanized thermoplastic elastomers (TPVs) based on polyamide‐6 (PA‐6) and poly(epichlorohydrin‐co‐ethylene oxide) (ECO) and their nanocomposites were prepared via melt‐blending process. The unfilled and organoclay (OC)‐filled TPVs were characterized using X‐ray diffraction (XRD), transmission electron microscopy (TEM), differential scanning calorimetry, thermal gravimetric analysis (TGA), and mechanical tests. XRD and TEM results showed that the OC particles were well exfoliated into the samples with high rubber content while both intercalated and exfoliated structures were found in the samples with low rubber content. The mechanical properties showed that ECO improved the elongation at break and the presence of OC increased the Young's modulus. Also, wide angle XRD analysis showed an increase in α‐crystals of PA‐6 with addition of ECO rubber. Moreover, it was found that by increasing OC content, crystallization temperature increased but the degree of crystallinity decreased. TGA showed that increasing ECO content decreased thermal stability of the samples, while the presence of OC did not have any considerable effect on the thermal stability. POLYM. COMPOS., 38:1948–1956, 2017. © 2015 Society of Plastics Engineers     

Effect of 1,1′‐dibenzyl‐4,4′‐bipyridyl dichloride (DBD) on charge‐conduction process and photovoltaic response of a polypyrrole (PPy) thin‐film device

The present communication deals with analysing the effect of 1,1′‐dibenzyl‐4,4′‐bipyridyl dichloride (DBD) substitution at the N‐position of 2,5‐polypyrrole (PPy), on electrical, impedance and photovoltaic properties. The thin‐film device was fabricated by sandwiching DBD‐substituted PPy between indium tin oxide (ITO) and aluminium (Al) electrodes. The formation of a Schottky barrier with Al and ohmic contact with ITO are explained in terms of p‐type semiconducting behaviour of DBD‐substituted PPy. In the low‐voltage region, Ohm's law is followed, while in the high‐voltage region, a space‐charge‐limited conduction (SCLC) controlled by the exponential‐trap distribution was observed. DBD substitution causes shifting of the Fermi level towards the valence‐band edge and an increase in charge‐carrier mobility. A remarkable change in dark electrical conductivity of the order of five has been observed in DBD‐substituted PPy. The electrical and impedance measurements of an ITO/PPy:DBD/Al device confirms the formation of a Schottky barrier at the DBD‐substituted PPy/Al interface. Additionally, it can be modelled by a simple equivalent circuit of two resistance–capacitance (RC) elements in series representing the bulk and a junction‐region. At low frequency, the device capacitance follows a pronounced voltage dependence. From a detailed analysis of the J–V and C–V characteristics, the ionized acceptor concentration (N_a), width of depletion layer (W) and potential barrier height (?_b) have been evaluated. We observed a significant enhancement in photocurrent on DBD substitution. The increase in photocurrent is explained by the efficient charge separation induced by the intermolecular transfer of photo‐excited electrons from PPy to DBD. The substitution also causes a reduction in the trapping centres in the material. © 2002 Society of Chemical Industry     

Electrical properties of FeII‐terpyridine‐Modified cellulose nanocrystals and polycaprolactone/FeII‐CTP nanocomposites

Supramolecular crosslinked Fe^II‐terpyridine cellulose nanocrystals (Fe‐CTP) were prepared by surface modification of cellulose nanocrystals with 4′‐chloro‐2,2′:6′,2″‐terpyridine and subsequent reaction with Fe(II)SO₄. The prepared complex was characterized using transmission electron microscopy (TEM), ultraviolet spectroscopy (UV), thermogravimetric analysis (TGA), and measuring its electrical properties at temperatures from 25 to 70°C. Use of Fe‐CTP at loadings from 1% to 10% (wt. ratio) in nanocomposites with polycaprolactone polymer was investigated; the nanocomposites were characterized regarding their electrical properties, which studied using broadband AC‐relaxation spectroscopy in the frequency range between 0.1 Hz and 1 MHz. The results were compared to that of PCL nanocomposites containing multiwalled carbon nanotubes (CNT). Variation in real and imaginary parts of permittivity has been explained on the basis of interfacial polarization of fillers in the polymer medium. The percolation limit of the conductive CNT and Fe‐CTP as studied by ac conductivity measurements has also been reported. Fe‐CTP showed conductivity values in the range of semiconductors. PCL/Fe‐CTP nanocomposites showed conductivity values from 1.98 × 10⁻¹¹ to 3.76 × 10⁻⁶ while PCL/CNT nanocomposites showed conductivity values from 1.4 × 10⁻¹⁰ to 3.67 × 10⁻⁴ S/m for 1–10 wt% CNT content. POLYM. COMPOS., 37:2734–2743, 2016. © 2015 Society of Plastics Engineers     

Dynamic properties of star‐shaped,solution‐polymerized styrene–butadiene rubber and its cocoagulated rubber‐filled with silica/carbon black

The dynamic properties, including the dynamic mechanical properties, flex fatigue properties, dynamic compression properties, and rolling loss properties, of star‐shaped solution‐polymerized styrene–butadiene rubber (SSBR) and organically modified nanosilica powder/star‐shaped styrene–butadiene rubber cocoagulated rubber (N‐SSBR), both filled with silica/carbon black (CB), were studied. N‐SSBR was characterized by ¹H‐NMR, gel permeation chromatography, energy dispersive spectrometry, and transmission electron microscopy. The results show that the silica particles were homogeneously dispersed in the N‐SSBR matrix. In addition, the N‐SSBR/SiO₂/CB–rubber compounds' high bound rubber contents implied good filler–polymer interactions. Compared with SSBR filled with silica/CB, the N‐SSBR filled with these fillers exhibited better flex fatigue resistance and a lower Payne effect, internal friction loss, compression permanent set, compression heat buildup, and power loss. The nanocomposites with excellent flex fatigue resistance showed several characteristics of branched, thick, rough, homogeneously distributed cross‐sectional cracks, tortuous flex crack paths, few stress concentration points, and obscure interfaces with the matrix. Accordingly, N‐SSBR would be an ideal matrix for applications in the tread of green tires. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40348.