Influence of oil contents in dynamically cured natural rubber and polypropylene blends

Mechanical, dynamic, thermal, and morphological properties of dynamically cured 60/40 NR/PP TPVs with various loading levels of paraffinic oil were investigated. It was found that stiffness, hardness, tensile strength, storage shear modulus, complex viscosity, glass transition temperature (T_g) of the vulcanized rubber phase, degree of crystallinity and crystalline melting temperature (T_m) of the polypropylene (PP) phase decreased with increasing loading levels of oil. This is attributed to distribution of oil into the PP and vulcanized rubber domains causing oil‐swollen amorphous phase and vulcanized rubber domains. An increasing trend of elastic response in terms of tension set and damping factor was observed in the TPVs with loading levels of oil in a range of 0–20 phr. It is supposed that a major proportion of oil was first preferably migrated into the PP phase and caused an abrupt decreasing trend of degree of crystallinity and T_m of the PP phase. The dispersed vulcanized rubber domains remained small as particles with a low degree of swelling. Increasing loading levels of oil higher than 20 phr caused a decreasing trend of elongation at break and elastomeric properties. Saturation of oil in the PP phase was expected and the excess oil was transferred to the rubber phase which thereafter caused larger swollen vulcanized rubber domains. The remaining amount of oil was able to separate as submicron pools distributed in the PP matrix. This caused lowering of T_g, T_m, crystallinity of PP phase as well as strength, elastomeric, and dynamic properties of the TPVs. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

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     

Development of hydroxyapatite nanoparticles reinforced chlorinated acrylonitrile butadiene rubber/chlorinated ethylene propylene diene monomer rubber blends

Hydroxyapatite nanoparticles (HA) reinforced polymer blend based on chlorinated nitrile rubber (Cl-NBR) and chlorinated ethylene propylene diene monomer rubber (Cl-EPDM) were prepared. Resulting blend composites were analyzed with regard to their rheometric processing, crystallinity, glass transition temperature (T_g), mechanical properties, oil resistance, AC conductivity, and transport behavior. The decrease in optimum cure time with the addition of HA is more advantageous for the development of products from these blend nanocomposites. The XRD, FTIR, and SEM confirmed the attachment and uniform dispersion of HA nanoparticles in the Cl-NBR/Cl-EPDM blend. The good compatibility between polymer blend and nanoparticles was also deduced by the formation of spherically shaped HA particles in the blend matrix determined by TEM analysis. DSC analysis showed an increase in T_g of the blend with the filler loading. The addition of HA particles to the blend produced a remarkable increase in tensile and tear strength, hardness, AC conductivity, abrasion, and oil resistance. The diffusion of blend composites was decreased with an increase in penetrant size. The diffusion mechanism was found to follow an anomalous trend. Among the blend composites, the sample with 7 phr of HA not only showed good oil and solvent resistance but also a remarkable increase in AC conductivity and mechanical properties.     

Effect of different nanoparticles on thermal,mechanical and dynamic mechanical properties of hydrogenated nitrile butadiene rubber nanocomposites

Organically modified and unmodified montmorillonite clays (Cloisite NA, Cloisite 30B and Cloisite 15A), sepiolite (Pangel B20) and nanosilica (Aerosil 300) were incorporated into hydrogenated nitrile rubber (HNBR) matrix by solution process in order to study the effect of these nanofillers on thermal, mechanical and dynamic mechanical properties of HNBR. It was found that on addition of only 4 phr of nanofiller to neat HNBR, the temperature at which maximum degradation took place (T_max) increased by 4 to 16°C, while the modulus at 100% elongation and the tensile strength were enhanced by almost 40–60% and 100–300% respectively, depending upon nature of the nanofiller. It was further observed that T_max was the highest in the case of nanosilica‐based nanocomposite with 4 phr of filler loading. The increment of storage modulus was highest for sepiolite‐HNBR and Cloisite 30B‐HNBR nanocomposites at 25°C, while the modulus at 100% elongation was found maximum for sepiolite‐HNBR nanocomposite at the same loading. A similar trend was observed in the case of another grade of HNBR having similar ACN content, but different diene level. The results were explained by x‐ray diffraction, transmission electron microscopy, and atomic force microscopy studies. The above results were further explained with the help of thermodynamics. Effect of different filler loadings (2, 4, 6, 8, and 16 phr) on the properties of HNBR nanocomposites was further investigated. Both thermal as well as mechanical properties were found to be highest at 8 phr of filler loading. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Physical–mechanical properties of carbon black–nanoclay composites of butyl rubber as curing bladder compounds

Abstract

Partial replacement of carbon black (CB) by organically modified montmorillonite (OMMT) in bladder compounds and synergistic effect between OMMT and CB on required properties were studied. X-ray diffraction results revealed intercalation of rubber into OMMT galleries. Mechanical interaction between rubber and filler, mechanical stability in oxidative aging, resistance to permanent set, reduction in permeation to CO₂, and resistance to thermal degradation were all in favour of clay containing composites, especially the compound with 45?phr CB and 4?phr OMMT.     

THE COMPARISON PROPERTIES OF RECYCLE RUBBER POWDER,CARBON BLACK,AND CALCIUM CARBONATE FILLED NATURAL RUBBER COMPOUNDS

The effects of filler loading on the curing characteristics, swelling behavior, and mechanical properties of natural rubber compounds were studied using a conventional vulcanization system. Recycle rubber powder (RRP), carbon black (CB) (N550), and calcium carbonate (CaCO₃) were used as fillers and the loading range was from 0 to 50 phr. Results show that the scorch time, t ₂, and cure time, t ₉₀, decrease with increase in filler loading. At a similar filler loading, RRP shows shortest t ₂ and t ₉₀ followed by CB and calcium carbonate. The tensile strength, tensile modulus, and hardness increase with increase in CB loading, whereas elongation at break, resilience, and swelling properties show opposite trend. For RRP and calcium carbonate filled natural rubber compounds, the tensile strength increases up to 10 phr and starts to deteriorate at higher filler loading. The other properties such as tensile modulus, hardness, elongation at break, resilience, and swelling percentage show a small change (increase or decrease) with increase in RRP and calcium carbonate loading in natural rubber compounds. Overall results indicate that RRP can be used as a cheapener to replace calcium carbonate in natural rubber compounds where improved mechanical properties are not critical.     

New approach for preparation of dry natural rubber nanocomposites through acid‐free co‐coagulation: Effect of organoclay content

Natural rubber (NR) vulcanizates exhibit good mechanical properties compared to vulcanizates of synthetic rubbers. Incorporation of a conventional filler at higher loadings to NR enhances its modulus, while reduction in tensile strength and elongation. This paper presents a new strategy for development of a NR‐clay nanocomposite with enhanced mechanical properties by incorporation of lower loadings (2–8 phr) of cetyl trimethyl ammonium bromide modified montmorillonite clay (OMMT‐C) under acid‐free environment. The effect of OMMT‐C loading on cure characteristics, rubber‐filler interactions, crosslink density, dynamic mechanical thermal properties, and mechanical properties were evaluated. Incorporation of OMMT‐C accelerated the vulcanization process and enhanced mechanical properties. X‐ray diffraction analysis and scanning electron microscopy images revealed that the formation of intercalated clay structures at lower OMMT‐C loadings, and clay aggregates at higher loadings. A nanocomposite at OMMT‐C loading of 2 phr exhibited the best balanced mechanical properties, and was associated with highest crosslink density and rubber–filler interactions. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46502.     

Curing characteristics and mechanical properties of rattan‐powder‐filled natural rubber composites as a function of filler loading and silane coupling agent

Curing characteristics, tensile properties, morphological studies of tensile fractured surfaces using scanning electron microscopy (SEM), and the extent of rubber filler interactions of rattan‐powder‐filled natural rubber (NR) composites were investigated as a function of filler loading and silane coupling agent (CA). NR composites were prepared by the incorporation of rattan powder at filler loading range of 0–30 phr into a NR matrix with a laboratory size two roll mill. The results indicate that in the presence of silane CA, scorch time (t_s2), and cure time (t₉₀) of rattan‐powder‐filled NR composites were shorten, while, maximum torque (M_H) increased compared with NR composites without silane CA. Tensile strength and tensile modulus of composites were enhanced whereas elongation at break reduced in the presence of silane CA mainly due to increase in rubber‐filler interaction. It is proven by SEM studies that the bonding between the filler and rubber matrix has improved. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Mechanical properties of blocked polyurethane/epoxy interpenetrating polymer networks

The mechanical properties of blocked polyurethane(PU)/epoxy interpenetrating polymer networks (IPNs) were studied by means of their static and damping properties. The studies of static mechanical properties of IPNs are based on tensile properties, flexural properties, hardness, and impact method. Results show that the tensile strength, flexural strength, tensile modulus, flexural modulus, and hardness of IPNs decreased with increase in blocked PU content. The impact strength of IPNs increased with increase in blocked PU content. It shows that the tensile strength, flexural strength, tensile modulus, and flexural modulus of IPNs increased with filler (CaCO₃) content to a maximum value at 5, 10, 20, and 25 phr, respectively, and then decreased. The higher the filler content, the greater the hardness of IPNs and the lower the notched Izod impact strength of IPNs. The glass transition temperatures (T_g) of IPNs were shifted inwardly compared with those of blocked PU and epoxy, which indicated that the blocked PU/epoxy IPNs showed excellent compatibility. Meanwhile, the T_g was shifted to a higher temperature with increasing filler (CaCO₃) content. The dynamic storage modulus (E′) of IPNs increased with increase in epoxy and filler content. The higher the blocked PU content, the greater the swelling ratio of IPNs and the lower the density of IPNs. The higher the filler (CaCO₃) content, the greater the density of IPNs, and the lower the swelling ratio of IPNs. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 1826–1832, 2006     

Enhancement in electrical and thermal performance of high-temperature vulcanized silicone rubber composites for outdoor insulating applications

High-temperature vulcanized silicone rubber composites are highly desirable as outdoor insulating materials due to their immense thermal and electrical performance. The aim of this work is to study the role of co-combined fillers (modified fumed silica [MFS], titanium dioxide [TiO₂], with graphene [G]) on electrical and thermal properties of silicone rubber (S) composites. The dielectric response of S/MFS_10 phr and S/TiO₂_20 composites tailored with 2 phr G was characterized by broadband dielectric spectroscopy. The hybrid filler/composites were found to show higher thermal stability when 2 phr G was added. In addition, a low quantity of G filler was found to slightly increase the AC dielectric breakdown strength of the S/MFS_10 and S/TiO₂_20, where an improvement of 3 and 5% was found, respectively. Several steps were observed in the thermal decomposition of the S rubber composites by thermogravimetric analysis-Fourier-transform infrared spectroscopy. Our findings revealed great potentials for fabricating hybrid-filler/silicone rubber composites with enhanced electrical and thermal properties for outdoor insulating applications.     

Influence of the clay modification and compatibilizer on the structure and mechanical properties of ethylene–propylene–diene rubber/montmorillonite composites

Ethylene–propylene–diene rubber (EPDM)/montmorillonite (MMT) composites were prepared through a melt process, and three kinds of surfactants with different ammonium cations were used to modify MMT and affect the morphology of the composites. The morphology of the composites depended on the alkyl ammonium salt length, that is, the hydrophobicity of the organic surfactants. Organophilic montmorillonite (OMMT), modified by octadecyltrimethyl ammonium salt and distearyldimethyl ammonium salt, was intercalated and partially exfoliated in the EPDM matrix, whereas OMMT modified by hexadecyltrimethyl ammonium chloride exhibited a morphology in which OMMT existed as a common filler. Ethylene–propylene–diene rubber grafted with maleic anhydride (MAH‐g‐EPDM) was used as a compatibilizer and greatly affected the dispersion of OMMT. When OMMTs were modified by octadecyltrimethyl ammonium chloride and distearydimethyl ammonium chloride, the EPDM/OMMT/MAH‐g‐EPDM composites (100/15/5) had an exfoliated structure, and they showed good mechanical properties and high dynamic moduli. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 92: 638–646, 2004     

Properties of Ferrite-Filled Natural Rubber Composites

Nickel zinc ferrite (Ni-ZnFe₂O₄)-filled natural rubber (NR) composite was prepared at various loading of ferrite. The tensile properties included in this study were tensile strength, tensile modulus and elongation at break. The tensile strength and elongation at break of the composites increased up to 40 parts per hundred rubber (phr) of ferrite and then decreased at higher loading whereas the tensile modulus was increased gradually with increasing of ferrite loading. Scanning electron microscopy (SEM) was used to determine the wettability of filler in rubber matrix. From the observation, the increase of filler loading reduced the wettability of the filler. Thermal stability of the composites was conducted by using a thermogravimetry analyser (TGA). The incorporation of ferrite in NR composites enhanced the thermal stability of NR composites. The swelling test results indicate that the swelling percentage of the composites decreased by increasing of ferrite loading. The initial permeability, μ_i and quality factor, Q of magnetic properties of NR composites achieved maximum value at 60 phr of ferrite loading for frequency range between 5000–40,000 kHz. The maximum impedance, Z _max of the NR composites was at the highest value at 80 phr ferrite loading for frequency range between 200–800 MHz.     

Effect of imidazolium ionic liquid type on the properties of nitrile rubber composites

We investigated the influence of hydrophilic and hydrophobic imidazolium ionic liquids on the curing kinetic, mechanical, morphological and ionic conductivity properties of nitrile rubber composites. Two room temperature ionic liquids with a common cation—1‐ethyl‐3‐methylimidazolium thiocyanate (EMIM SCN; hydrophilic) and 1‐ethyl‐3‐methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIM TFSI; hydrophobic)—were used. Magnesium–aluminium layered double hydroxide (MgAl‐LDH; also known as hydrotalcite) was added to carboxylated acrylonitrile–butadiene rubber (XNBR) whereas fumed silica Aerosil 380 was used in acrylonitrile–butadiene rubber (NBR) as reinforcing fillers. NBR compounds were vulcanized with a conventional sulfur‐based crosslinking system whereas XNBR compounds were cured with MgAl‐LDH. The optimum cure time reduction and tensile properties improvement were obtained when both ionic liquids were added at 5 parts per hundred rubber (phr). The results revealed that EMIM SCN and EMIM TFSI induced an increase in the AC conductivity of nitrile rubber composites from 10^?10 to 10^?8 and to 10^?7 S cm^?1, respectively (at 15 phr ionic liquid concentration). The presence of ionic liquids in NBR slightly affected the glass transition temperature (T_g) whereas the presence of EMIM TFSI in XNBR contributed to a shift in T_g towards lower temperatures from ?23 to ?31 °C, at 15 phr loading, which can be attributed to the plasticizing behaviour of EMIM TFSI in the XNBR/MgAl‐LDH system. Dynamic mechanical analysis was also carried out and the related parameters, such as the mechanical loss factor and storage modulus, were determined. © 2013 Society of Chemical Industry     

Structure and properties of polybutadiene/montmorillonite nanocomposites prepared by in situ polymerization

Polybutadiene (PB)/Montmorillonite nanocomposites (NCs) were prepared by in situ polymerization through the anionic polymerization technique. The effects of treating method of organophilic MMT (OMMT), the type of OMMT, and the solvent used in polymerization were studied. The structure and properties of NCs were characterized using X‐ray Diffraction (XRD), transmission electron micrograph (TEM), H‐NMR spectrum, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and dynamic mechanical analysis (DMA). The consumption of BuLi was varied with different treating methods. The molecular weight distribution of PB added with OMMT (DK1) was wide, and the molecular weight distribution became narrow when OMMT‐DK1B and DK4 were added. OMMT did not disperse stably in cyclohexane, but could form a homogeneous solution in toluene and xylene. XRD and TEM showed that exfoliated NCs were obtained by in situ polymerization through the anionic polymerization technique. From the H‐NMR spectrum of PB and PB/OMMT NCs, it could be seen that the content of 1, 2 units of PB increased ～100%, while 1, 4 units decreased when 6.2 wt % of OMMT was added. The results of DSC and DMA indicated that T_g and T_dc were increased when compared with those of PB. Both storage modulus and loss modulus were increased with the addition of OMMT, and tan δ was decreased. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 99: 3615–3621, 2006     

Properties of silica/clay filled heavy‐duty truck tire thread formulation

A tire thread formulation for heavy‐duty trucks containing SBR/BR rubber blend and varying proportions of silica/clay fillers including a silane‐coupling agent have been investigated. The various mixes were compounded in a Banbury ‘O’ mixer and vulcanized using the EV‐system. Silica/clay (80/0) served as the control mix. The oscillating disc rheometer (ODR) was used in determination of cure characteristics. Substitution of silica (80 phr) with china clay up to 40 phr increased the cure rate of the rubber blend mixes as well as their maximum torque level (T_max). T_max was observed to be highest at a filler blend ratio of 40/40 phr. Synergism between silica and clay at this filler blend mixture is suggested to be responsible for the observation. The heat buildup was reduced from 43 to 20°C as the clay content increased. Results also showed that the rubber blend compound containing silica/clay (60/20) filler blend in the stated ratio exhibited the best balance of properties in the critical parameters such as the absolute torque level (69.5 dNm), heat buildup (39°C), and abrasion resistance (0.574 mg.loss/1,000 rev). The rate of depreciation of abrasion resistance of rubber blend compound as the clay content increased was found to be 0.035 mg loss/1,000 rev as silica is substituted with one part of china clay phr. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 94: 1024–1028, 2004     

Dynamic Mechanical Properties of Carbon Black Filled Ethylene Vinyl Acetate Rubber

Abstract

The dynamic mechanical properties of ethylene vinyl acetate (EVA) rubber filled with different loadings of carbon black and at different degrees of crosslinking were studied over a wide range of temperatures (-150° to +200°C). The loss tangent (tan δ) versus temperature plots indicated presence of different transitions. The α-transition (or the glass-rubber transition) corresponding to the maximum in tan δ value, occurred at ?17°C, which is the principal glass-transition temperature (abbreviated as T _g) of EVA rubber. The γ-transition occurred in the temperature region of ?125° to ?135°C, while the β-transition appeared as a shoulder in the temperature region of ?65° to ?75°C. Besides, there was also a high tempeature transition around +62°C which is known as liquid to liquid transition (T _1.1). Incorporation of carbon black filler did not cause any shift of T _g, while the tan δ peak values at T _g decreased sequentially with increase in filler loading. The γ- and β-relaxations were found to be insensitive to filler loading. The T _1.1 transition, however, was found to be suppressed by incorporation of carbon black filler particularly at high loading. Extent of crosslinking did not influence the T _g But, the T _1.1 transition, which was prominent with the lightly crosslinked system was found to be suppressed at high level of crosslinking. Strain dependent dynamic mechanical properties under isothermal conditions showed that the secondary structure breakdown of carbon black filler under the effect of strain amplitude is influenced by the degree of crosslinking of EVA rubber.     

A Comparative Study on Curing Characteristics,Mechanical Properties,Swelling Behavior,Thermal Stability,and Morphology of Feldspar and Silica in SMR L Vulcanizates

Abstract

Comparison studies on effects of feldspar and silica (Vulcasil C) as a filler in (SMR L grade natural rubber) vulcanizates on curing characteristics, mechanical properties, swelling behavior, thermal analysis, and morphology were examined. The incorporation of both fillers increases the scorch time, t ₂, and cure time, t ₉₀, of SMR L vulcanizates. At a similar filler loading, feldspar exhibited longer t ₂ and t ₉₀ but lower values of maximum torque, M_HR, and torque difference, M_HR–M_L than did silica-filled SMR L vulcanizates. For mechanical properties, both fillers were found to be effective in enhancing the tensile strength (up to 10 phr), tensile modulus, and hardness of the vulcanizates. However, feldspar-filled SMR L vulcanizates showed lower values of mechanical properties than did silica-filled SMR L vulcanizates. Swelling measurement indicates that swelling percentages of both fillers-filled SMR L vulcanizates decrease with increasing filler loading whereas silica shows a lower swelling percentage than feldspar-filled SMR L vulcanizates. Scanning electron microscopy (SEM) on fracture surface of tensile samples showed poor filler–matrix adhesion for both fillers with increasing filler loading in the vulcanizates. However, feldspar-filled SMR L vulcanizates showed poorer filler–matrix adhesion than did silica-filled SMR L vulcanizates. Thermogravimetric analysis (TGA) results indicate that the feldspar-filled SMR L vulcanizates have higher thermal stability than do silica-filled SMR L vulcanizates.     

Properties of styrene butadiene rubber (SBR)/recycled acrylonitrile butadiene rubber (NBRr) blends: The effects of carbon black/silica (CB/Sil) hybrid filler and silane coupling agent,Si69

The recycling or reuse of waste rubber by means of blending together with polymeric materials in addition of filler such as hybrid carbon black and silica (CB/Sil) to a polymer system can provides an opportunity to explore alternative product specifications. Therefore, in this work the investigation of recycled rubber blends based on styrene butadiene rubber/recycled acrylonitrile butadiene rubber (SBR/NBRr) blends reinforced with 50/0, 40/10, 30/20, 20/30, 40/10, 0/50 phr of carbon black/silica (CB/Sil) hybrid filler treated with and without silane coupling agent (Si69) were determined. Cure characteristics, tensile properties, and morphological behavior of selected SBR/NBRr blends at a fix 85/15 blend ratio were evaluated. Results showed that, cure time t₉₀, minimum torque (M_L), and maximum torque (M_H) of CB/Sil hybrid fillers filled SBR/NBRr blends with and without Si69 increased as silica content increased. However, t₉₀ and M_L of SBR/NBRr blends with Si69 were lower than without Si69 except for (M_H). The optimum scorch time (t_s2) of SBR/NBRr blends with and without Si69 was obtained at 30/20 phr of CB/Sil hybrid filler. However, t_s2 of SBR/NBRr blends with Si69 were longer than SBR/NBRr blends without Si69. The incorporation of Si69 has improved the tensile properties [(tensile strength, elongation at break (E_b), stress at 100% elongation (M100), and stress at 300% elongation (M300)] of CB/Sil hybrid fillers filled SBR/NBRr blends. These properties were influenced by the degree of crosslinked density as the silica content is increased. Scanning electron microscopy (SEM) of the tensile fracture surfaces indicated that, with the addition of Si69 improved the dispersion of hybrid fillers and NBRr in SBR/NBRr matrix. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Torrefied agro-industrial residue as filler in natural rubber compounds

This study explored the feasibility of using torrefied biomass as a reinforcing filler in natural rubber compounds. Carbon black was then replaced with the torrefied biomass in elastomer formulations for concentrations varying from 0% to 100% (60 parts per hundred rubber or phr total). Their influence on the curing process, dynamic properties, and mechanical properties was investigated. Results were compared with the properties of vulcanizates containing solely carbon black fillers. Time to cure (t₉₀) for compounds with torrefied biomass fillers increased, while filler-filler interactions (ΔG') decreased, compared to carbon black controls. At low strains, the tan δ values of the torrefied fillers vulcanizates were similar to the controls. Incorporation of torrefied biomass into natural rubber decreased compound tensile strength and modulus but increased elongation. Replacement with torrefied fillers resulted in a weaker filler network in the matrix. Still, results showed that moderate substitution concentrations (~20 phr) could be feasible for some natural rubber applications.     

Cure Characteristics,Mechanical and Thermal Properties of Al2O3 and ZnO Reinforced Silicone Rubber

The effects of alumina (Al₂O₃) and zinc oxide (ZnO) fillers on the curing characteristics, thermal and mechanical properties of silicone rubber were studied. Rheometer results indicate that the incorporation of ZnO fillers retards the curing process, whereas an enhancement in cure rate was observed for Al₂O₃. Higher maximum torque (M_H) and minimum torque (M_L) values was also observed for ZnO silicone rubber compounds compared to Al₂O₃. Thermogravimetric analysis (TGA) showed that ZnO silicone rubber compounds are thermally more stable than Al₂O₃; however, the coefficient of thermal expansion of the Al₂O₃ silicone rubber compounds are lower than that of ZnO. Comparison in mechanical strength between the two silicone rubber hybrids indicates that ZnO is a better reinforcement filler, as evidenced in the tensile strength, elongation at break, and modulus at 300% elongation.