Effect of Carbon Black/Silica Hybrid Filler on Thermal Properties,Fatigue Life,and Natural Weathering of SBR/Recycled NBR Blends

The utilization of nitrile glove waste will spark a great deal of interest in the rubber industry in developing cost-effective techniques to convert waste and used rubber into a processable form. Blends of styrene butadiene rubber/recycled acrylonitrile butadiene rubber (SBR/NBRr) reinforced at 85/15 blend with different ratios of a carbon black/silica (CB/Sil) hybrid filler (50/0, 40/10, 30/20, 20/30, 40/10, 0/50 phr) were tested either with or without the silane coupling agent, Si69. Results showed that the increased thermal stability of blends with Si69 is highly related to the formation of crosslinks between the filler. Thermogravimetric (TG) thermograms showed that the percentage of char residue for blends with Si69 was higher than without Si69. The differential scanning calorimetry (DSC) thermograms of both blends revealed a glass transition temperature (Tg) between 65.0°C and 66.9°C. At all blend ratios, the fatigue life of blends with Si69 was better than blends without Si69. After six months’ exposure to natural weather, blends with Si69 exhibited better tensile properties, retention, and morphology compared to blends without Si69.     

The Effect of Electron Beam (EB) Irradiation in Presence of TMPTA on Cure Characteristics and Mechanical Properties of Styrene Butadiene Rubber/Recycled Acrylonitrile-Butadiene Rubber (SBR/NBRr) Blends

The effect of electron beam (EB) irradiation on the cure characteristics and mechanical properties of unirradiated and irradiated SBR/NBRr blends were investigated. The SBR/NBRr blends were prepared at 95/5, 85/15, 75/25, 65/35, and 50/50 blend ratio with and without the presence of a polyfunctional monomer, trimethylolpropane triacrylate (TMPTA). Results indicated that the scorch time t₂, cure time t₉₀ and minimum torque (M_L) of irradiated SBR/NBRr blend decreased, but the maximum torque (M_H) particularly at 35 and 50 phr of NBRr (recycled NBR) increased with the presence of TMPTA. The stress at 100% elongation (M100), hardness, cross-linking density and tensile strength (particularly after 15 phr of NBRr content) of irradiated SBR/NBRr blends increased after irradiation but the elongation at break (EB) and resilience decreased. The irradiated SBR/NBRr blends showed lower thermal stability than non-irradiated blends. Scanning electron microscopy proved the enhancement in tensile strength when more NBRr were added in SBR matrix where the irradiated surfaces demonstrate more irregularity with increasing crack branching (fracture planes are located at different heights) due to the increased of cross-linked density.     

Effect of epoxidized natural rubber on thermal properties,fatigue life,and natural weathering test of styrene butadiene rubber/recycled acrylonitrile‐butadiene rubber (SBR/NBRr) blends

The utilization of waste rubber powder in polymer matrices provides an attractive strategy for polymer waste disposal. Addition of recycled acrylonitrile‐butadiene rubber (NBRr) in rubber compounds gives economic (lowering the cost of rubber compounds) as well as processing advantages. In this study, the properties of styrene butadiene rubber (SBR)/NBRr blends with and without epoxidized natural rubber (ENR‐50) as a compatibilizer were determined. The results such as thermal gravimetric analysis (TGA), fatigue life, and natural weathering test of SBR/NBRr blends with and without ENR‐50 were carried out. Results showed that TG thermograms of SBR/NBRr blends with ENR‐50 show lower thermal stability compared blends without ENR‐50. The incorporation of ENR‐50 into SBR/NBRr blends has reduced char residue compared SBR/NBRr blends without ENR‐50. The incorporation of ENR‐50 in SBR/NBRr blends has increased the rigidity of the blends thus lowering the fatigue life. The increment in tensile properties retention of SBR/NBRr blends with ENR‐50 indicated the enhancement on weathering resistant. The surfaces of SBR/NBRr blends with ENR‐50 after 6 months exposure showed a minimal severity of crack compared with SBR/NBRr blends without ENR‐50. It revealed that the scale of cracks has reduced indicating well‐retaining interfacial adhesion between SBR and NBRr with the presence of ENR‐50 as a compatibilizer. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Preparation and properties of styrene‐butadiene rubber nanocomposites blended with carbon black‐graphene hybrid filler

Graphene has become an attractive reinforcing filler for rubber materials, but its dispersion in rubber is still a big challenge. In this work, a novel carbon black‐reduced graphene (CB‐RG) hybrid filler was fabricated and blended with styrene‐butadiene rubber (SBR) via simple two‐roll mill mixing. The prepared CB‐RG hybrids had a microstructure with small CB agglomerates adsorbed onto graphene surfaces. CB acted as a barrier preventing the RG sheets from restacking even after drying. Homogeneous dispersion of graphene sheets in SBR matrix was observed by the mechanical mixing method based on the application of the CB‐RG hybrid fillers. Dynamic mechanical analysis showed that Tg of the SBR/CB‐RG blend was higher than that of the SBR/CB blend indicating strong interfacial interactions between RG and SBR due to the high surface area of graphene and the π‐π interaction between SBR and graphene. The tensile properties of SBR/CB‐RG composites improved significantly and the volume resistivity decreased compared with the SBR/CB blends. The thermal stability of SBR composites filled with CB and CB‐RG showed slight difference. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41309.     

Mechanical reinforcement in magadiite/styrene‐butadiene rubber composites

This work investigates mechanical properties of styrene‐butadiene rubber (SBR) composites incorporating magadiite (MGD), a synthetic layered silicate (Na₂Si₁₄O₂₉·9H₂O) with surface chemistry similar to precipitated silica used in tire tread formulations. Treatment with cetyltrimethylammonium (CTA⁺) expands the MGD layers and makes the interlayer face surfaces accessible to sulfur‐functional silane TESPT (Si69) and SBR, primarily during batch mixing. DMA and tensile testing of cured CMGD/SBR composites show that CTA‐treated MGD (CMGD) provides substantially higher levels of mechanical reinforcement than equivalent amounts of silica. However, CMGD/SBR composites exhibit larger loss tangent values above T_g, probably due to lower SBR‐SBR crosslink density resulting from interlayer trapping of sulfur released by Si69 during vulcanization. DMA and tensile testing also demonstrate Si69′s critical role in forming MGD‐SBR graft sites essential to mechanical reinforcement. Replacing silica with CMGD reduces composite weight without sacrificing tensile modulus, suggesting that use of CMGD in tire rubber formulations could improve vehicle energy efficiency. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44763.     

Effect of carbon black loading on curing characteristics and mechanical properties of waste tyre dust/carbon black hybrid filler filled natural rubber compounds

Curing characteristics, tensile properties, fatigue life, swelling behavior, and morphology of waste tire dust (WTD)/carbon black (CB) hybrid filler filled natural rubber (NR) compounds were studied. The WTD/CB hybrid filler filled NR compounds were compounded at 30 phr hybrid filler loading with increasing partial replacement of CB at 0, 10, 15, 20, and 30 phr. The curing characteristics such as scorch time, t₂ and cure time, t₉₀ decreased and increased with increment of CB loading in hybrid filler (30 phr content), respectively. Whereas maximum torque (M_HR) and minimum torque (M_L) increased with increasing CB loading. The tensile properties such as tensile strength, elongation at break, and tensile modulus of WTD/CB hybrid filler filled NR compounds showed steady increment as CB loading increased. The fatigue test showed that fatigue life increased with increment of CB loading. Rubber–filler interaction, Q_f/Q_g indicated that the NR compounds with the highest CB loading exhibited the highest rubber–filler interactions. Scanning electron microscopy (SEM) micrographs of tensile and fatigue fractured surfaces and rubber–filler interaction study supported the observed result on tensile properties and fatigue life. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

The role of interlayer grafting on the mechanical properties of magadiite/styrene‐butadiene rubber composites

This work examines the mechanisms by which magadiite (MGD), a synthetic layered silicate, acts as an active filler to provide high levels of mechanical reinforcement in styrene‐butadiene rubber (SBR) composites. Cetyltrimethylammonium (CTA⁺) expands the MGD layer spacing and promotes intercalation of SBR and silane coupling agent (Si69); the resulting CMGD/SBR composites have greater tensile moduli than comparable silica/SBR composites. CMGD was reacted in solution with Si69 (or MPTES) to prepare “pre‐grafted” MGD with varying levels of interlayer silane functionalization (SMGD). If the silane graft density is relatively low, the resulting SMGD/SBR composite has mechanical properties comparable to CMGD composites prepared with Si69 added during batch mixing. However, SMGD with high silane graft density does not permit SBR intercalation and produces composites with inferior mechanical properties, demonstrating the necessity of silane‐mediated interlayer grafting. Omitting Si69 from the formulation dramatically reduces the level of mechanical reinforcement as measured by DMA and tensile testing. Adding extra bulk sulfur (to replace sulfur omitted with Si69) does not produce composites with mechanical properties comparable to CMGD/SBR or SMGD/SBR prepared with Si69. This work demonstrates that silane‐mediated SBR‐MGD grafts within the MGD interlayer space are essential for achieving high levels of mechanical reinforcement in MGD/SBR composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45025.     

Effect of different types of filler and filler loadings on the properties of carboxylated acrylonitrile–butadiene rubber latex films

The effects of different types of fillers and filler loadings on the properties of carboxylated nitrile rubber (XNBR) latex were identified. Silica, mica, carbon black (CB; N330), and calcium carbonate (CaCO₃) were used as fillers with filler loadings of 10, 15, and 20 parts per hundred rubber. Furnace ashing and Fourier transform infrared analysis proved that interaction existed between the fillers and XNBR latex films. The morphology of the filled XNBR films was significantly different for different types of fillers. Mica and CaCO₃ fillers showed uneven distribution within the XNBR film, whereas other fillers, such as silica and CB, showed homogeneous distribution within the films. In the observation, silica and mica fillers also illustrated some degree of agglomeration. The mechanical properties (e.g., tensile and tear strengths) showed different trends with different types of fillers used. For silica and mica fillers, the mechanical properties increased with filler loadings up to a certain loading, and decreased with higher filler loadings. For CB filler, the mechanical properties increased gradually with increasing filler loadings. CaCO₃ fillers did not increase the mechanical properties. The crosslinking density of the XNBR films increased when they were incorporated with fillers because of the presence of elastomer–filler and filler–filler interactions. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Preparation and characterization of poly(styrene‐co‐butadiene) and polybutadiene rubber/clay nanocomposites

Poly(styrene‐co‐butadiene) rubber (SBR) and polybutadiene rubber (BR)/clay nanocomposites have been prepared. The effects of the incorporation of inorganically and organically modified clays on the vulcanization reactions of SBR and BR were analysed by rheometry and differential scanning calorimetry. A reduction in scorch time (t_s1) and optimum time (t₉₅) was observed for both the rubbers when organoclay was added and this was attributed to the amine groups of the organic modifier. However, t_s1 and t₉₅ were further increased as the clay content was increased. A reduction in torque value was obtained for the organoclay nanocomposites, indicating a lower number of crosslinks formed. The organoclays favoured the vulcanization process although the vulcanizing effect was reduced with increasing clay content. The tensile strength and elongation of SBR were improved significantly with organoclay. The improvement of the tensile properties of BR with organoclay was less noticeable than inorganic‐modified clay. Nevertheless, these mechanical properties were enhanced with addition of clay. The mechanical properties of the nanocomposites were dependent on filler size and dispersion, and also compatibility between fillers and the rubber matrix. Copyright © 2004 Society of Chemical Industry     

A Study of FTIR,Thermal Properties and Natural Weathering Test on NBRVirgin/Recycled with SBR Blends

The effects of styrene butadiene rubber/virgin acrylonitrile butadiene rubber (SBR/NBRv) blends and styrene butadiene rubber/recycled acrylonitrile butadiene rubber (SBR/NBRr) blends on properties such Fourier transform infrared (FTIR), thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC) were carried out. Results indicated that, based on intensity of amine peak from FTIR at 85/15 blend ratio (R15) revealed optimum formation of crosslink between SBR and NBR either using virgin or NBRr. TG thermograms of SBR/NBRv blends of all ratios showed better onset thermal stability than SBR/NBRr blends. The change in the horizontal baseline from high to low energy level occurred in virgin NBR blends because the amount of reactive sites available in virgin NBR is higher compared to NBRr. Meanwhile NBRr blends showed T_c because the amount of crosslink occurred in these blends were slightly lower than NBRv blends. Up to 25 phr of NBRr, the tensile strength and elongation at break (E_b) retention of SBR/NBRv blends was better than SBR/NBRr blends after 6 months' weathering test except for M100. The scanning electron microscopy on the surface of both blends after 6 months exposure indicated that the severity of the crack was minimal for SBR/NBRr blends compared to SBR/NBRv particularly at 50/50 blend ratio designated the SBR/NBRr blends that contained more NBRr particles could reduce the degradation towards natural weathering.     

Thermal and scanning electron microscopy/energy‐dispersive spectroscopy analysis of styrene–butadiene rubber–butadiene rubber/silicon dioxide and styrene–butadiene rubber–butadiene rubber/carbon black–silicon dioxide composites

Silica as a reinforcement filler for automotive tires is used to reduce the friction between precured treads and roads. This results in lower fuel consumption and reduced emissions of pollutant gases. In this work, the existing physical interactions between the filler and elastomer were analyzed through the extraction of the sol phase of styrene–butadiene rubber (SBR)–butadiene rubber (BR)/SiO₂ composites. The extraction of the sol phase from samples filled with carbon black was also studied. The activation energy (E_a) was calculated from differential thermogravimetry curves obtained during pyrolysis analysis. For the SBR–BR blend, E_a was 315 kJ/mol. The values obtained for the composites containing 20 and 30 parts of silica per hundred parts of rubber were 231 and 197 kJ/mol, respectively. These results indicated an increasing filler–filler interaction, instead of filler–polymer interactions, with respect to the more charged composite. A microscopic analysis with energy‐dispersive spectroscopy showed silica agglomerates and matched the decreasing E_a values for the SBR–BR/30SiO₂ composite well. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 2273–2279, 2005     

Effect of pulverized coal/carbon black hybrid fillers on mechanical properties and thermal stability of styrene butadiene rubber composites

Pulverized coal (coal) possesses a layered structure similar to graphite and is a potential reinforcing filler. In this paper, ball milling is used to reduce the particle diameter of coal. The coal is modified with KH-560 to obtain K-COAL and prepared K-COAL/styrene-butadiene rubber (SBR) composites. In addition, carbon black (CB) is modified to obtain CB-Si69, K-COAL and CB-Si69 are added to SBR in different ratios to prepare COAL/CB/SBR composites. The results show that the addition of K-COAL can improve the vulcanization performance, thermal stability, and mechanical properties of SBR composites, but the reinforcing effect is weak. In the COAL/CB/SBR composites, the vulcanization and mechanical properties of the composites gradually increase with the increase of CB, while those of the thermal stability decrease. The tensile strength of the 10 phr COAL/30 phr CB/SBR composite is 24.1 MPa, which is elevated by 1105% and 205% compared with the pure SBR and 40 phr K-COAL/SBR composites, respectively. The composites maintain high elasticity while the tensile strengths are greatly improved, and the mechanical properties are significantly enhanced. In conclusion, this paper provides a reference for the clean utilization of coal and shows new possibilities for finding new fillers to replace CB.     

Effect of silane coupling agent on the structure and mechanical properties of nano‐dispersed clay filled styrene butadiene rubber

In rubber nanocomposites containing inorganic clay, the reinforcement effect has always been relatively insignificant due to the poor interfacial interaction between the rubber matrix and clay fillers. In this work, the silane coupling agent bis[3‐(triethoxysilyl)propyl]tetrasulfide (Si‐69) was employed through mechanically blending with styrene butadiene rubber (SBR)/clay (100/30) nanocompound that was prepared by combined latex compounding and spray‐drying technique, to serve as the molecular bridge between SBR matrix and clay filler and strengthen the interfacial interaction. TEM and XRD characterization indicated that Si‐69 significantly improved the dispersion of the silicate layers in the SBR matrix. The RPA analysis and the mechanical property study of the SBR/clay nanocomposites revealed that the filler network interaction was weakened while the filler–rubber interaction was strengthened upon the addition of Si‐69. POLYM. COMPOS., 37:890–896, 2016. © 2014 Society of Plastics Engineers     

Natural Weathering Test of Styrene Butadiene Rubber and Recycled Acrylonitrile Butadiene Rubber (SBR/NBRr) Blends

The effect of recycled acrylonitrile butadiene rubber (NBRr) content of SBR/NBRr blends on natural weathering was studied. Three different size of NBRr (S1; 117–334 µm, S2; 0.85–15.0 mm and S3; direct sheeted form) were used and the blends were exposed to natural weathering for 3 and 6 months. The results indicated that the SBR/NBRr blends with smallest size of NBRr (S1) show a better retention of tensile properties, which are able to withstand better weathering than coarser size (S2 and S3) of SBR/NBRr blends. The presence of hydroxyl, carbonyl and nitro group after exposure to natural weathering was detected in FTIR analysis, which related to the UV oxidation process of rubber blends. The scanning electron microscopy proved that the SBR/NBRr blends with smallest size of NBRr (S1) with higher content of NBRr, shows a better resistant to natural weathering.     

BIMS/filler interactions. I. Effects of filler structure

Polymer/filler interactions have been found to affect the performance of tire tread, sidewall, innerliner, or carcass and other industrial rubber products that are all based on filled elastomers. Identification of types of various polymer/filler interactions and ranking of their impacts have been elusive. Isobutylene-based polymers have relatively saturated structures and contain very low concentrations of functional group. Examples are BIMS (a brominated isobutylene/p-methylstyrene copolymer) containing p-bromomethylstyrene and p-methylstyrene; bromobutyl rubber containing  Br and olefin; chlorobutyl rubber containing  Cl and olefin; and butyl rubber containing olefin. On the other hand, high diene rubbers, such as polybutadiene rubber, polyisoprene rubber, and styrene/butadiene rubber, have unsaturated backbones and high olefin contents. Hence, different types and extents of interaction with reinforcing fillers, such as carbon black (CB) or silica, are expected in these two classes of elastomer. This work employs bound rubber (solvent extraction), viscoelasticity, stress–strain measurements, and solid state NMR to identify, differentiate, and scale polymer/filler interactions in unvulcanized BIMS/CB, BIMS/silica, SBR/CB, and SBR/silica composites, where SBR denotes a styrene/butadiene rubber. Four different types of CB and one type of silica have been studied. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 4943–4956, 2006     

Regulation of trans‐1,4‐polyisoprene crystallinity and mechanical properties of styrene‐butadiene rubber/trans‐1,4‐polyisoprene vulcanizate

The effects of processing temperature and bis‐[γ‐(triethoxysilyl)‐propyl]‐tetrasulfide (Si69) on crystallization, morphology, and mechanical properties of styrene‐butadiene rubber (SBR)/trans‐1,4‐polyisoprene (TPI) vulcanizate are investigated. The crystallinity and crystalline melting temperature (T_m) of TPI in the vulcanizates with TPI/silica/(Si69) pre‐mixed at 150 °C are much lower than that pre‐mixed at 80 °C. At the same pre‐mixing temperature, the presence of 1 phr Si69 leads to a decreased crystallinity and T_m. The TPI domains with phase size of about 1 μm and silica are well dispersed in the vulcanizate, and TPI crystals get smaller in size and less in amount by pre‐mixing TPI, silica and Si69 at 150 °C. The vulcanizates with TPI/silica/(Si69) pre‐mixed at 150 °C have decreased tensile strength and modulus at a given extension than that pre‐mixed at 80 °C. At the same pre‐mixing temperature, the tensile strength and modulus of the vulcanizate increase with the addition of 1 phr Si69. The crystallinity of TPI component in SBR/TPI vulcanizate is effectively controlled by changing processing temperature and adding Si69, which is important for theoretical research and practical application of TPI. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44395.     

Styrene butadiene rubber/epoxidized natural rubber/carbon filler nanocomposites: microstructural development and cure characterization

Microstructural development of elastomeric nanocomposites based on (50/50 wt%) styrene butadiene rubber (SBR) and epoxidized natural rubber (50 mol% epoxidation, ENR50) as the rubber matrix including two types of carbon fillers, carbon black (CB) and functionalized multiwall carbon nanotube (NH₂-MWCNT), which were prepared through melt mixing, was studied. The results from FTIR analysis show that there is interaction between functional groups on MWCNT surface and the rubber chains. The AFM analysis also indicates good dispersion of filler particles in the rubber phases. FESEM images from cryo-fractured surface of samples have revealed that nanotubes were rarely pulled out of matrix and their diameter increased, resulting from good interaction between MWCNTs and rubber chains. The DMA results confirm good interfacial interaction between them. Furthermore, the reduced difference between the two T_gs of phases (ΔT_g) shows that the incorporation of 3 phr MWCNT into the blend leads to increment in rubber phase compatibility but at higher MWCNT content (5 phr) due to lower Mooney viscosity of SBR phase, MWCNTs tend to remain in this phase. The bound rubber was adopted to characterize the polymer–filler interaction, showing that bound rubber content has an increasing trend with increasing in fillers content. The cure rheometric studies reveal that MWCNTs accelerate the cure process due to the presence of amine groups on the nanotube surface. In addition, the mechanical properties of samples show an increasing trend by increasing nano-filler content.

     

Curing Characteristics and Mechanical and Morphological Properties of Styrene Butadiene Rubber/Virgin Acrylonitrile-Butadiene Rubber (SBR/vNBR) and Styrene Butadiene Rubber/Recycled Acrylonitrile-Butadiene Rubber (SBR/rNBR) Blends

Curing characteristics and mechanical and morphological properties of styrene butadiene rubber/virgin acrylonitrile-butadiene rubber (SBR/vNBR) and styrene butadiene rubber/recycled acrylonitrile-butadiene rubber (SBR/rNBR) were investigated. Results indicated that the curing characteristics, such as scorch time, t₂, and cure time, t₉₀, of SBR/vNBR and SBR/rNBR blends decreased with increasing vNBR and rNBR content. At similar blend ratios, particularly up to 15 phr, SBR/rNBR blends exhibited higher t₂ and t₉₀ compared with SBR/vNBR blends. Minimum torque (ML) and maximum torque (MH) of SBR/vNBR blends significantly increased with increasing vNBR content. For SBR/rNBR blends, ML increased with increasing rNBR content, but MH exhibited the opposite trend. Tensile strength, elongation at break (E_b), resilience, and fatigue decreased with increasing virgin and recycled NBR content in both blends. Up to 15 phr, the tensile strength, E_b and fatigue life (Kc) of SBR/rNBR blends were higher than in SBR/vNBR blends. The M100 (stress at 100% elongation), hardness, and cross-linking density of both blends also showed an increasing trend with increasing vNBR and rNBR content. The scanning electron microscopy study indicates that rNBR exhibited a weak rNBR-SBR matrix interaction particularly when more than 15 phr of rNBR was used, thus decreasing the mechanical properties of SBR/rNBR blends.     

Effect of filler loading on cure time and swelling behaviour of SMR L/ENR 25 and SMR L/SBR blends

The effect of filler loading on the cure time (t₉₀) and swelling behaviour of SMR L/ENR 25 and SMR L/SBR blends has been studied. Carbon black (N330), silica (Vulcasil C) and calcium carbonate were used as fillers and the loading range was from 0 to 40 phr. Results show that for SMR L/ENR 25 blends the cure time decreases with increasing carbon black loading, whereas silica shows an increasing trend, and calcium carbonate does not show significant changes. For SMR L/SBR blends, the cure time of carbon black, silica and calcium carbonate generally decreases with increasing filler loading. The percentage swelling in toluene and ASTM oil no 3 decreases for both blends with increasing filler loading, with calcium carbonate giving the highest value, followed by silica‐ and carbon black‐filled blends. At a fixed filler loading, SMR L/ENR 25 blend shows a lower percentage swelling than SMR L/SBR blends. © 2003 Society of Chemical Industry     

Norbornylized soybean oil as a sustainable new plasticizer for rubbers with hybrid fillers

Carbon black (CB) and precipitated silica are two major reinforcing fillers in rubbers. CB/silica hybrid filler is also widely used in rubbers to provide balanced properties. CB/silica‐hybrid‐filler‐filled styrene‐butadiene rubber (SBR) containing naphthenic oil (NO), soybean oil (SO) and norbornylized SO (NSO) was investigated. The swelling and curing behavior and rheological, mechanical, thermal, aging and dynamic properties were studied and compared with earlier reported data on CB‐ or silica‐filled SBR. NSO provides better scorch safety and faster cure than SO. Compared with NO, the addition of SO and NSO enhances the thermal stability and aging resistance of SBR vulcanizates. SBR/NSO vulcanizates with hybrid filler exhibit a higher tensile and tear strength than SBR/NO and SBR/SO vulcanizates. A synergistic effect in the abrasion resistance of vulcanizates containing the hybrid filler is observed. An increase of sulfur content in the hybrid‐filler‐filled SBR/NSO vulcanizates provides further improvement in abrasion resistance, wet traction and rolling resistance. © 2017 Society of Chemical Industry