Keratin as a filler for carboxylated acrylonitrile‐butadiene rubber XNBR

The presented investigations concern the distribution and characterization of keratin waste, derived from the processes of cattle skins, and its use as a filler for carboxylated acrylonitrile‐butadiene rubber XNBR. The recovered keratin improves mechanical proprieties such as tensile strength, hardness, resistance to fuel and oil. The addition of keratin in a quantity of five parts per hundred rubber (XNBR) increases the crosslinking density of composites, as testified by the formed ion nodes and the existing mono and disulphide bonds. Electric conductance and water absorption increased with time for elastomers filled with protein. Therefore these composites are biodegradable after their period of use. As a result hydrophilic–hydrophobic protein–elastomeric composites will have usable properties. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

细菌纤维素填充的水刺激-力响应羧基丁腈橡胶复合膜

采用浇铸法通过将细菌纤维素晶须(BCW)与羧基丁腈橡胶胶乳(XNBR)混合制备了BCW/XNBR橡胶复合膜,研究了该膜的吸水性能及吸水前后常温储能模量的变化.结果表明,随着时间延长,BCW/XNBR膜的吸水速率减小,约3d达到溶胀平衡状态.随着BCW用量的增加,BCW/XNBR膜的平衡溶胀程度增大,当BCW为10份(质量)时膜的吸水质量分数最大达到18％.吸水后BCW/XNBR膜的常温储能模量显著降低,加入10份BCW时较吸水前降低了87.3％,这表明BCW/XNBR膜具有良好的水刺激-力响应性能.     

Properties of silica‐filled styrene‐butadiene rubber compounds containing acrylonitrile‐butadiene rubber: The influence of the acrylonitrile‐butadiene rubber type

Because silica has strong filler‐filler interactions and adsorbs polar materials, a silica‐filled rubber compound exhibits poor dispersion of the filler and poor cure characteristics in comparison with those of a carbon black‐filled rubber compound. Acrylonitrile‐butadiene rubber (NBR) improves filler dispersion in silica‐filled styrene‐butadiene rubber (SBR) compounds. The influence of the NBR type on the properties of silica‐filled SBR compounds containing NBR was studied with NBRs of various acrylonitrile contents. The composition of the bound rubber was different from that of the compounded rubber. The NBR content of the bound rubber was higher than that of the compounded rubber; this became clearer for NBR with a higher acrylonitrile content. The Mooney scorch time and cure rate became faster as the acrylonitrile content in NBR increased. The modulus increased with an increase in the acrylonitrile content of NBR because the crosslink density increased. The experimental results could be explained by interactions of the nitrile group of NBR with silica. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 385–393, 2002     

Investigation of electrically conductive acrylonitrile‐butadiene rubber

Electrically conductive acrylonitrile‐butadiene rubbers (NBRs) containing carbon black (CB) as conductive filler were prepared in order to investigate their electrical and mechanical properties. The effects of conductive CB loading, temperature, acrylonitrile content, crosslinking density of vulcanizates, and plasticizer on conductivity were studied. The change in electrical conductivity of NBRs with different amounts of CB showed that there is a certain critical point (percolation threshold) where a significant decrease in electrical resistivity (increase in conductivity) is observed. Mechanical properties such as tensile strength, elongation to break, and surface hardness of vulcanized NBRs were measured. It was found that the percolation threshold was 5 phr of CB for the NBR/CB composites. J. VINYL ADDIT. TECHNOL., 13:71–75, 2007. © 2007 Society of Plastics Engineers.     

Impact of blend ratio on the properties of graphene oxide‐filled carboxylated acrylonitrile–butadiene rubber/styrene–butadiene rubber blends

Carboxylated acrylonitrile–butadiene rubber (XNBR) and styrene–butadiene rubber (SBR) composites with 3 phr (parts per hundred rubber) graphene oxide (GO) were prepared using a latex mixing method. Effects of XNBR/SBR blend ratios on the mechanical properties, thermal conductivity, solvent resistance and thermal stability of the XNBR/SBR/GO nanocomposites were studied. The tensile strength, tear strength, thermal conductivity and solvent resistance of the XNBR/SBR/GO (75/25/3) nanocomposite were significantly increased by 86, 96, 12 and 21%, respectively, compared to those of the XNBR/SBR (75/25) blend. The thermal stability of the nanocomposite was significantly enhanced; in other words, the temperature for 5% weight loss and the temperature of the maximal rate of degradation process were increased by 26.01 and 14.97 °C, respectively. Theoretical analysis and dynamic mechanical analysis showed that the GO tended to locate in the XNBR phase, which led to better properties of the XNBR/SBR/GO (75/25/3) nanocomposite. © 2017 Society of Chemical Industry     

Mechanical and viscoelastic behavior of natural rubber and carboxylated styrene‐butadiene rubber latex blends

The morphology, mechanical and viscoelastic behavior of latex blends of unvulcanized natural rubber (NR) with carboxylated styrene‐butadiene rubber (XSBR) were investigated, with special reference to the effect of the blend ratio, temperature, and frequency. Mechanical properties like tensile strength, modulus, and elongation at break were also studied. As the XSBR content increased, the tensile strength increased up to a 50:50 NR/XSBR ratio and then decreased as a result of the self‐curing nature of XSBR. The dynamic mechanical properties of these latex blends were analyzed for loss tangent, storage modulus, and loss modulus. The entire blend yielded two glass‐transition temperatures, which corresponded to the transitions of individual components, indicating that the system was immiscible. To determine the change in modulus with time, a master curve of 50:50 NR/XSBR blends was plotted. Time–temperature superposition and Cole–Cole analysis were done to understand the phase behavior of the latex blends. The experimental and theoretical values of storage modulus of blends were compared using the Kerner and Halpin–Tsai models. With the help of optical micrographs, attempts were made to correlate the morphology and viscoelastic behavior of these blends. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 2639–2648, 2003     

Electron‐beam curing of hydrogenated acrylonitrile–butadiene rubber

The electron‐beam‐induced crosslinking of hydrogenated acrylonitrile–butadiene rubber (HNBR) was investigated. HNBR sheets were exposed to electron‐beam irradiation in air at a room temperature of 25 ± 2°C over a dose range of 0–20 Mrad. An attempt was made to correlate the structure of the irradiated rubber with the properties. The ratio of chain scission to crosslinking and the gelation dose were determined by a method proposed elsewhere. The gel content and dynamic storage modulus increased with the radiation dose. Fourier transform infrared studies revealed the formation of double bonds and carbonyl and ether groups. These observations were further supported by a thermogravimetric analysis of the carbonaceous residue of irradiated HNBR. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 648–651, 2005     

Hydrogenation of acrylonitrile–butadiene rubber latexes

The hydrogenation of acrylonitrile–butadiene rubber (NBR) latex was carried out by a system consisting of hydrazine hydrate and hydrogen peroxide, with boric acid as catalyst. Highly saturated hydrogenated NBR (HNBR) latex was obtained through the optimization of the reaction conditions. The dried HNBR was found to be heavily gelled. The cause for the crosslink of dried hydrogenated NBR products was investigated. With the improvement of the hydrogenation system, that is, by adding gel inhibitor to the system, the crosslinking was controlled to a large extent, and dried HNBR with gel content of about 3% was prepared by the improved system. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 91: 2072–2078, 2004     

Improvement of properties of silica‐filled styrene–butadiene rubber compounds using acrylonitrile–butadiene rubber

Since silica has strong filler–filler interactions and adsorbs polar materials, a silica‐filled rubber compound has a poor dispersion of the filler and poor cure characteristics. Improvement of the properties of silica‐filled styrene–butadiene rubber (SBR) compounds was studied using acrylonitrile–butadiene rubber (NBR). Viscosities and bound rubber contents of the compounds became lower by adding NBR to the compound. Cure characteristics of the compounds were improved by adding NBR. Physical properties such as modulus, tensile strength, heat buildup, abrasion, and crack resistance were also improved by adding NBR. Both wet traction and rolling resistance of the vulcanizates containing NBR were better than were those of the vulcanizate without NBR. The NBR effects in the silica‐filled SBR compounds were compared with the carbon black‐filled compounds. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 79: 1127–1133, 2001     

Swelling and mechanical properties of (acrylonitrile‐butadiene rubber)/(hydrogenated acrylonitrile‐butadiene rubber) blends with precipitated silica filled in gasohol fuels

This work studied the effects of hydrogenated acrylonitrile‐butadiene rubber (HNBR) and precipitated silica (PSi) loadings in acrylonitrile‐butadiene rubber (NBR) filled with 60 parts per hundred of rubber (phr) of carbon black (CB) for oil‐resistant seal applications in contact with gasohol fuel. The cure characteristics, mechanical properties, and swelling behavior of HNBR/NBR blends reinforced with PSi before and after immersion in ethanol‐based oils (E10, E20, and E85) were then monitored. This work studied the effects of PSi loading in rubber compounds on the mechanical properties of the rubber blends. The results suggested that the scorch time of CB‐filled NBR/HNBR was not affected by HNBR loading, but the cure time, Mooney viscosity, and torque difference increased with HNBR content. The swelling of the blends in E85 oil were relatively low compared with those in E10 and E20 oils. The recommended NBR/HNBR blend ratio for oil‐resistant applications was 50/50. Tensile strength and elongation at break before and after immersion in gasohol oils increased with HNBR loading, and the opposite effect was found for tensile modulus and hardness. PSi filler had no effect on scorch time, but decreased the cure time of the blends. The swelling level of the blends slightly decreased with increasing PSi content. The recommended silica content for optimum reinforcement for black‐filled NBR/HNBR blend at 50/50 was 30 phr. The results in this work suggested that NBR/HNBR blends reinforced with 60 phr of CB and 30 phr of silica could be potentially used for rubber seals in contact with gasohol fuels. J. VINYL ADDIT. TECHNOL., 22:239–246, 2016. © 2014 Society of Plastics Engineers     

Nanomodified fillers in chloroprene‐rubber‐compatibilized natural rubber/acrylonitrile–butadiene rubber blends

Because of the structural dissimilarity, natural rubber (NR) and acrylonitrile–butadiene rubber (NBR) are immiscible, and compatibilizers are used during their blending. Neoprene or chloroprene rubber (CR) has a polar chlorine part and a nonpolar hydrocarbon part. Also, it has many advantageous properties, such as oil resistance, toughness, a dynamic flex life, and adhesion capacity. Hence, it is not less scientific to use CR as a compatibilizer in the blending of NBR with NR. Because many fewer studies on the use of neoprene as a compatibilizer in NR–NBR blend preparation are available, efforts were made to prepare 20:80 NR–NBR blends with CR with the aim of studying the effect of poly(ethylene oxide) (PEO)‐coated nano calcium silicate along with nano N‐benzylimine aminothioformamide and stearic acid coated nano zinc oxide in the sulfur vulcanization of the blends. The optimum dosage of the compatibilizer was derived by the determination of the tensile properties, tear resistance, abrasion resistance, compressions set, and swelling values. The tensile strength, tear resistance, and abrasion resistance of the gum vulcanizates of the blend were improved by the compatibilizing action of CR up to 5 parts per hundred parts of rubber (phr). In the case of the filled vulcanizates, the tear resistance, 300% modulus, hardness, and abrasion resistance increased with increasing dosage of nano calcium silicate. The elongation at break percentage decreased as expected when there was an increase in the modulus. Scanning electron microscopy was used to study the phase morphology of the blends. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Mechanical properties and microstructure of acrylonitrile–butadiene rubber vulcanizates reinforced by in situ polymerized phenolic resin

The phenolic resin (PF) was incorporated into acrylonitrile–butadiene rubber (NBR) vulcanizates by in situ polymerization during the vulcanization process. It was found that the tensile strength, tearing strength, and tensile strength (300% elongation) could be considerably enhanced 59.4, 80.2, and 126.4%, respectively, at an optimum PF content of only 15 phr, but the elongation at break and shore A hardness were only slightly affected on the basis of silica‐reinforced NBR vulcanizates. A systematic study of the PF structure formed within the NBR matrix using various experimental schemes and procedures has revealed that the PF resin would form the localized discontinuous three‐dimensional interconnected network structures in the NBR matrix. The substantial reinforcement of PF on the mechanical properties of vulcanized NBR were attributed to the morphology, high flexibility, and moderate stiffness of the PF phases and their excellent bonding with rubbers through “rubber to rubber” and interface layer. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Electron‐beam irradiation of blends of polypropylene with recycled acrylonitrile‐butadiene rubber

One‐mm thick sheets were prepared from blends of polypropylene and recycled acrylonitrile‐butadiene rubber (rNBR) with different blend ratios. Trimethylolpropane triacrylate (TMPTA) was used as a co‐agent. Electron‐beam‐initiated cross‐linking of the sheets was carried out at a dose of 40 kGy, and 3 phr of TMPTA based on the weight of rNBR was used. Properties such as tensile strength, Young's modulus, elongation at break, swelling percentage in oil, and morphology were studied. The results showed that the tensile properties had been improved by irradiation. The studies of swelling in oil revealed a higher cross‐link density in the irradiated blends compared to that in nonirradiated blends at similar blend ratios. Scanning electron microscopy studies revealed better adhesion between the phases and rough failure surfaces with a large number of tear lines which indicated a higher energy requirement for the failure of irradiated blends compared to that for nonirradiated blends. J. VINYL ADDIT. TECHNOL., 2010. © 2010 Society of Plastics Engineers     

Water induced stiff-soft transition of butadiene-styrene rubber/bacterial cellulose whiskers nano-composites prepared by three different approaches

正Materials responding to small variation of environmental conditions by the change of their properties such as mechanical properties and electrical properties are known as stimuli-responsive materials.They have drawn great interests in both academia and industry owing to their various potential applications.Recently,researchers made natural rubber/reduced graphene oxide nano-composites prepared by waterbased solution casting.The results showed that the nano-composites     

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     

Amelioration of acrylonitrile–butadiene copolymer properties using natural rubber graft p‐aminophenol

A two‐roll mill machine was used for the grafting of p‐aminophenol (pAP) onto natural rubber (NR). The prepared NR graft p‐aminphenol (NR‐g‐pAP) was characterized by ¹H NMR and IR spectroscopy techniques. The goal of this article is to study the effect of commercial antioxidants, N‐phenyl‐N′‐(1,3‐dimethylbutyl)‐p‐phenylenediamine (6PPD) and N‐phenyl‐N′‐isopropyl‐p‐phenylenediamine (IPPD), and the prepared NR‐g‐pAP, on the mechanical properties of acrylonitrile–butadiene (NBR) vulcanizates, the fluid compatibility of NBR vulcanizates, the hydraulic brake and clutch fluid dot, the diffusion out for NBR vulcanizate components, and the compression recovery of NBR vulcanizates. This study indicates that the NBR copolymer vulcanizate which contains the prepared NR‐g‐pAP has good protection against mechanical stress and the diffusion out of NBR vulcanizate components. The 6PPD and the prepared NR‐g‐pAP ameliorates the fluid compatibility of the oil seals, which is based on NBR as elastomer, and the hydraulic brake and clutch fluid dot. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Fracture behaviour of acrylonitrile–butadiene rubber/clay nanocomposite

A new fracture behaviour is described for acrylonitrile–butadiene rubber/clay nanocomposite. The nanocomposite is prepared by melt mixing the organo‐treated montmorillonite into the rubber matrix, together with a peroxide curative, and crosslinked by conventional compression moulding for typical rubbers. A considerable enhancement in stiffness is observed without serious sacrifice in ultimate strength. A totally different tear morphology of a series of regularly‐spaced tear ridges parallel to the direction of tearing was observed instead of the typical ‘cross‐hatched morphology’ of conventional rubber composites. © 2001 Society of Chemical Industry     

Effect of adding carbon fiber on conductive stability of acrylonitrile‐butadiene rubber composites

In this work, the conductive composites of acrylonitrile‐butadiene rubber (NBR) and conductive carbon black (CCB) were prepared. The volume resistivity of NBR/CCB composites became stable when the addition content of CCB reached 12 wt %. However, when carbon fiber (CF) was added into the composites, the volume resistivity of NBR/CCB/CF composites continued to decrease with the increase of CF addition, which resulted from the formation of the three‐dimensional conductive network in composite matrix. In addition, the effect of acid oxidation of CF surface on the mechanical proprieties and conductive stability of NBR/CCB/CF composites was studied. The results indicated the acid oxidation of CF surface improved the bond structure between NBR and CF, which further decreased the resistance and significantly improved the mechanical properties of the composites. It was demonstrated that the conductive stability of NBR composites after cyclic mechanical and temperature fatigues was remarkably enhanced with the addition of CF. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46668.     

Rheological behavior of nanocomposites of natural rubber and carboxylated styrene butadiene rubber latices and their blends

Flow behavior of latices is industrially important for the manufacturing of various latex goods. Rheology of latices having fillers can assist in the understanding and quantification of the matrix–filler interaction. The impact of layered silicates such as sodium bentonite and sodium fluorohectorite on the rheological behavior of natural rubber, carboxylated styrene butadiene rubber latices, and their blends was analyzed with special reference to shear rate, temperature, and filler loading. The layered silicates‐reinforced latex samples were characterized by X‐ray diffraction technique to analyze the extent of intercalation and exfoliation. In the presence of layered silicates, latex systems exhibited enhancement in viscosity due to the network formation. Because of the breaking of networks at higher temperature, the viscosity of all systems decreased with increase in temperature. Layered silicates‐reinforced latex systems showed pseudoplastic flow behavior and possesses enhanced zero shear viscosity and yield stress. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2355–2362, 2006     

Mechanical properties and network structure of phenol resin crosslinked hydrogenated acrylonitrile‐butadiene rubber

The tough and stretchable crosslinked hydrogenated acrylonitrile–butadiene rubber (HNBR) could be prepared by resol type phenol resin as a crosslinker. The mechanical properties and the network structure of the phenol resin crosslinked HNBR were investigated by comparing with those of the peroxide crosslinked HNBR having the higher crosslink density and the heterogeneous network structure. The elastic modulus and the strain at break of the phenol resin crosslinked HNBR were much higher than those of the peroxide one. The residual strain was below 20 % after stretching up to 650 % and then releasing from the cramps. Since the crosslink density is low, the high elastic modulus and the good recovery deformation are attributed to the stiffness and rigidity of the crosslink junctions obtained by phenol resin. Small‐angle X‐ray scattering measurements revealed that the network structure is spatially homogeneous and the results of the wide angle X‐ray diffraction indicate that the strain‐induced crystallization is suppressed, which enable the longer elongation. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013