Academic literature on the topic 'Rubber tear strength'

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Journal articles on the topic "Rubber tear strength"

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Hamed, G. R. "Tearing of Vulcanized Rubber." Rubber Chemistry and Technology 78, no. 3 (July 1, 2005): 548–53. http://dx.doi.org/10.5254/1.3547896.

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Abstract This short review summarizes some results of studies of rubber fracture carried out in the author's laboratory over the past several years. Particular attention has been focused on the details of cracking in technically important natural rubber vulcanizates with very high resistance to tearing. Such rubbers develop auxiliary cracks that grow essentially parallel to the loading direction and inhibit the main tear front from advancing. This crack splitting is attributed to oriented structure at the tear front and is predicted to occur when strength anisotropy at a tear tip reaches a critical value.
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Medalia, Avrom I. "Effect of Carbon Black on Ultimate Properties of Rubber Vulcanizates." Rubber Chemistry and Technology 60, no. 1 (March 1, 1987): 45–61. http://dx.doi.org/10.5254/1.3536121.

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Abstract In this survey, we have concluded that carbon black reinforces ultimate properties of rubber by tear deviation. This can occur at the colloidal level, as the tear is forced to pass around carbon black aggregates, thus increasing the area of the torn surface. Colloidal tear deviation may be the cause of the increase in threshold tearing energy which appears to be a small but significant component of reinforcement. Most reinforcement under ordinary test conditions is due to macroscopic tear deviation. This appears to be caused by strands of carbon black aggregates which force the growing tear to change direction. Macroscopic tear deviation is readily observed in a trouser tear test as stick-slip or knotty tear. In the tensile strength test, tear deviation prevents catastrophic rupture until a high stress is reached. In order to be effective in this or other ultimate properties, the carbon black must not debond; i.e., failure must go through the rubber rather than through the debonded rubber—filler interface. Reinforcing carbon blacks do not debond (from diene rubbers) under normal conditions and so do not require further strengthening of the rubber—filler bonds.
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Gibala, D., D. Thomas, and G. R. Hamed. "Cure and Mechanical Behavior of Rubber Compounds Containing Ground Vulcanizates: Part III. Tensile and Tear Strength." Rubber Chemistry and Technology 72, no. 2 (May 1, 1999): 357–60. http://dx.doi.org/10.5254/1.3538807.

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Abstract A black-filled styrene-butadiene rubber (SBR) vulcanizate was ambiently ground, then used as an additive to the original, uncured compound. Sheets of the resulting composite (matrix/ground rubber particulate) were cured, and tensile and trouser tear strength determined. The composite had reduced tensile strength, but enhanced tear strength relative to the original vulcanizate. The contrasting behavior is attributed to the effects of sulfur migration into the particulate rubber and differences in the responses of a tensile and a tear testpiece to discontinuities. In brief, ground rubber acts as a stress-raising flaw in tensile testing, while promoting crack tip blunting and stick-slip behavior in trouser tearing.
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Gent, A. N., S.-M. Lai, C. Nah, and Chi Wang. "Viscoelastic Effects in Cutting and Tearing Rubber." Rubber Chemistry and Technology 67, no. 4 (September 1, 1994): 610–18. http://dx.doi.org/10.5254/1.3538696.

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Abstract Measurements of cutting resistance have been made for a crosslinked styrene—butadiene copolymer over a wide range of cutting speeds and temperatures. A characteristic fracture energy was determined using the procedure of Lake and Yeoh. A lower limit, about 150 J/m2, was obtained at low cutting speeds. This value is significantly higher than the threshold tear strength, about 30 J/m2, due to roughness of the blade tip. The tear resistance increased dramatically as the test temperature was lowered, by a factor of over 1000X, whereas the cutting resistance remained largely unchanged over a considerable temperature range. Much of the enhanced tear resistance at low temperatures is therefore attributed to increasing roughness of the tear tip, the intrinsic strength remaining approximately constant. As the tear strength followed a WLF temperature dependence closely, roughening of the tear tip is associated with viscoelastic effects. Higher cutting resistance was shown by a sulfur vulcanizate, but carbon black had no additional effect. Variations in tensile strength with rate of elongation and temperature are discussed in terms of tearing from an initial edge flaw.
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Skrobak, Adam, Michal Stanek, David Manas, Martin Ovsik, Vojtech Senkerik, and Martin Reznicek. "Mechanical Properties of Rubber Samples." Key Engineering Materials 606 (March 2014): 249–52. http://dx.doi.org/10.4028/www.scientific.net/kem.606.249.

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This article demonstrates what influence has a change in production technology on mechanical properties of rubber testing samples. It compares two basic production technologies compression molding and injection molding. The aim of this research is to show and evaluate to what extent the properties (tensile strength, extension, tear strength and microhardness) are influenced by the used production technology and to quantify this potential difference on the basis of standard tests. The mechanical tension test according the standard ISO 37, the test determining tear strength according to the standard ISO 34-1 and the instrumented microhardness test (DSI) according to the standard ISO 6507-1.
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Hongkeab, Tarakol, and Peerapan Dittanet. "Mechanical Behavior of Polystyrene-Grafted Natural Rubber/Natural Rubber Blend: Effect of Polystyrene Grafting Percentage." Key Engineering Materials 751 (August 2017): 308–13. http://dx.doi.org/10.4028/www.scientific.net/kem.751.308.

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Polystyrene-grafted natural rubber (PS-GNR) at various graft levels was evaluated to improve mechanical properties of natural rubber (NR). PS-GNR was synthesized by emulsion copolymerization at 60°C at different reaction times between 15 and 360 mins to control the grafting levels of PS in the PS-GNR co-polymer. The resultant PS-GNR co-polymers were then blended into NR latex. The vulcanized NR compounds were investigated for the effect of PS grafting percentage in PS-GNR/NR compounds on mechanical properties, including tensile, tear strength and hardness. A core-shell structure was revealed with PS encapsulating the NR core via transmission electron microscopy. The polystyrene grafting percentage was determined to be 12.7%, 17.1%, 22.1% and 23.6% for polymerization times of 15 min, 60min, 120min, and 360 min, respectively. Addition of PS-GNR into NR exhibited biphasic behavior, resulting in a decrease in the tensile strength and tear strength. With further increase in grafting percentage of PS, the tensile strength and tear strength continues to decrease. The rigid chain of PS grafted onto NR surface reduced the elasticity of NR chain resulting in lower tear strength and the tensile strength. Fracture surface revealed a decrease in ductility of material with increasing grafting percentage of PS. On the other hand, modulus and hardness of PS-GNR/NR compounds were found to increase with increasing grafting percentage of PS. The addition of PS-GNR to rubber compound had shown an impact on dynamic behavior. With further increase in grafting percentage of PS in PS-GNR, an enhancement of storage modulus of rubber compound was clearly observed.
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Jana, G. K., and C. K. Das. "Mechanochemical Devulcanization of Vulcanized Gum Natural Rubber." Progress in Rubber, Plastics and Recycling Technology 21, no. 3 (August 2005): 183–99. http://dx.doi.org/10.1177/147776060502100302.

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De-vulcanization of vulcanized elastomers represents a great challenge because of their three-dimensional network structure. Sulfur-cured gum natural rubbers containing three different sulfur/accelerator ratios were de-vulcanized by thio-acids. The process was carried out at 90 °C for 10 minutes in an open two-roll cracker-cum-mixing mill. Two concentrations of de-vulcanizing agent were tried in order to study the cleavage of the sulfidic bonds. The mechanical properties of the re-vulcanized rubber (like tensile strength, modulus, tear strength and elongation at break) were improved with increasing concentrations of de-vulcanizing agent, because the crosslink density increased. A decrease in scorch time and in optimum cure time and an increase in the state of cure were observed when vulcanized rubber was treated with high amounts of de-vulcanizing agent. The temperature of onset of degradation was also increased with increasing concentration of thio-acid. DMA analysis revealed that the storage modulus increased on re-vulcanization. From IR spectroscopy it was observed that oxidation of the main polymeric chains did not occur at the time of high temperature milling. Over 80% retention of the original mechanical properties (like tensile strength, modulus, tear strength and elongation at break) of the vulcanized natural rubber was achieved by this mechanochemical process.
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Bhowmick, Anil K., Chanchal Neogi, and S. P. Basu. "Threshold tear strength of carbon black filled rubber vulcanizates." Journal of Applied Polymer Science 41, no. 56 (1990): 917–28. http://dx.doi.org/10.1002/app.1990.070410504.

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Hamed, G. R., and M. Y. Huang. "Tensile and Tear Behavior of Anisotropic Double Networks of a Black-Filled Natural Rubber Vulcanizate." Rubber Chemistry and Technology 71, no. 5 (November 1, 1998): 846–60. http://dx.doi.org/10.5254/1.3538513.

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Abstract Double networks of a black-filled natural rubber composition have been prepared by partially curing a sheet, stretching it, and then completing cure. Upon release, a double network retracts to a residual extension ratio, αr. Samples cut perpendicular to the stretch direction have stress—strain responses like the isotropic single network, while parallel samples have enhanced stiffness and tensile strength, and reduced extensibility. Tensile strength is rather weakly dependent on αr. Tear strengths of the double networks, determined using edge-cut strip specimens, exceed that of the single network for low αr. However, when αr is high, double networks have very low tear strengths. Consistent with previous studies, high tear strengths are associated with extensive longitudinal cracking.
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Petrović, Zoran S., Jelena Milić, Mihail Ionescu, and James R. Halladay. "EPDM RUBBER PLASTICIZED WITH POLYMERIC SOYBEAN OIL OF DIFFERENT MOLECULAR WEIGHTS." Rubber Chemistry and Technology 90, no. 4 (October 1, 2017): 667–82. http://dx.doi.org/10.5254/rct.18.82690.

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ABSTRACT Polymerization of soybean oil produces higher-viscosity liquids, which may serve as processing aids and plasticizers in certain rubbers as a replacement of petrochemical oils. Four polymerized soybean oils of different molecular weights showed good compatibility with ethylene–propylene–diene rubber (EPDM), but because of the presence of double bonds and copolymerization with EPDM, they decreased the cross-linking density when compared with paraffinic extender oil. As a consequence, polymeric soybean oils reduced tensile strength and modulus but increased elongation, tear strength, and compression set. Higher-molecular-weight plasticizers are expected to reduce sweating out of oils. Pure soybean oil was not completely compatible at the concentration tested, but it showed a strong plasticizing effect; dramatically lowered tensile strength, tear strength, and modulus; and increased elongation and compression set. No clear effect of molecular weight of polymerized soybean oils on properties was observed, but increasing the sulfur content was found to be beneficial. Using polymeric vegetable oils instead of petrochemical extenders in EPDM rubbers is economical and environmentally desirable, but the curing system requires optimization to accommodate loss of cross-linking density.
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Dissertations / Theses on the topic "Rubber tear strength"

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Samsuri, A. B. "Tear strength of filled rubbers." Thesis, London Metropolitan University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.234798.

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Hiza, Sarah B. "The Effect of Aging and Aging Under Stress on the Tear Strength of Filled Natural Rubber Vulcanizates." University of Akron / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=akron1134576240.

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Adepetun, Adeyemi Adedayo. "Effect of Carbon Black Loading and Temperature on Cut Growth in N990-Filled Natural Rubber Vulcanizates." University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1315575370.

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Books on the topic "Rubber tear strength"

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Institution, British Standards. Rubber and plastics: Analysis of multi-peak traces obtained in determinations of tear strength and adhesion strength. London: B.S.I., 1998.

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Samsuri, Azemi Bin. Tear strength of filled rubbers. 1989.

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Book chapters on the topic "Rubber tear strength"

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 77 COMPOUND FOR TEAR STRENGTH." In The Rubber Formulary, 543. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50335-3.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 40 COMPOUND FOR TEAR STRENGTH." In The Rubber Formulary, 101. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50031-2.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 74, WET TRACTION, TEAR STRENGTH." In The Rubber Formulary, 134–35. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50056-7.

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Ciullo, Peter A., and Norman Hewitt. "COMPOUND FOR TEAR STRENGTH, ABRASION RESISTANCE." In The Rubber Formulary, 167. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50087-7.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 60, HEAT RESISTANCE & TEAR STRENGTH." In The Rubber Formulary, 105. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50035-x.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 60, TEAR STRENGTH & HEAT RESISTANCE." In The Rubber Formulary, 236. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50146-9.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 70, TEAR STRENGTH & HEAT RESISTANCE." In The Rubber Formulary, 237. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50147-0.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 60, TEAR STRENGTH, LOW HEAT BUILD-UP." In The Rubber Formulary, 106–7. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50036-1.

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Ciullo, Peter A., and Norman Hewitt. "DUROMETER 73 COMPOUND FOR ABRASION RESISTANCE, HIGH VISCOSITY AND TEAR STRENGTH." In The Rubber Formulary, 163. Elsevier, 1999. http://dx.doi.org/10.1016/b978-081551434-3.50084-1.

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I. Gumede, Jabulani, James Carson, and Shanganyane P. Hlangothi. "Carbon Nanotubes as Reinforcing Nanomaterials for Rubbers Used in Electronics." In Carbon Nanotubes - Redefining the World of Electronics [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.94061.

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The field of electronics involves complex systems where the active and passive electronic devices are integrated on the rubber substrate, e.g., silicone (Q), which provides, through potting, a strong assembly of these devices on the circuit board. Several other rubbers are employed in the field to strengthen, insulate and seal the components of the electronic machines and instruments, and therefore protect them against damage. These rubbers are typically strengthened and toughened using carbon black (CB). However, due to its noticeable drawbacks, recent research in the field of rubber and electronics has suggested the use of carbon nanotubes (CNTs) as alternative reinforcing fillers to produce electronics rubber composites that do not only have enhanced electrical conductiv¬ity, thermal stability, electromagnetic interference (EMI) shielding, weatherability and insulation properties, but also offer outstanding stretchability, bendability and tear strength under frequent elastic deformation. These performances are similar for both single-walled carbon nanotubes (SWCNTs) and multi-walled carbon nanotubes (MWCNTs) in both the functional and structural composites. Although SWCNTs can result in relatively better homogeneity than MWCNTs, most rubbers often constitute MWCNTs because they are relatively cheaper. The great potential of rubber-CNTs composites being extensively used in the field of electronics is explored in this chapter.
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Conference papers on the topic "Rubber tear strength"

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Georgescu, Mihai, Maria Sonmez, Laurentia Alexandrescu, Mihaela Nituica, Maria Daniela Stelescu, and Dana Gurau. "Designing and obtaining wood waste and chloroprene rubber-based composites." In The 8th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2020. http://dx.doi.org/10.24264/icams-2020.iv.7.

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The aim of this paper is to obtain and study the properties of wood waste reinforced elastomer composites with various fibre contents (10-50 wt%). The composite is based on chloroprene rubber, and added post-consumer recycled wood particles, with dimensions of 500 nm eco-reinforcing material, and active fillers, plasticizers, vulcanizing agents, antioxidants. In order to enhance the compatibility and their level of interaction, the wood waste was finely ground (cryogenic mill) and functionalized with potassium oleate. Wood waste acts as a filling material which leads to the biodegradability of the composite and the decrease in density. Tensile, tear strength, elasticity, hardness, abrasion resistance, melt flow index and morphological study (FT-IR) of those composites were examined in order to determine the viability in various applications domains.
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Stelescu, Maria Daniela, Daniela Ioana Constantin, Maria Sonmez, Laurentia Alexandrescu, Mihaela Nituica, and Mihai Georgescu. "Development of elasto-plastic eco-nano-materials for the footwear industry." In The 8th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2020. http://dx.doi.org/10.24264/icams-2020.iv.22.

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The paper refers to the obtaining of new types of eco-nano elasto-plastic materials with high-performance characteristics based on ethylene-propylene-terpolymer rubber (EPDM), high-density polyethylene (HDPE), plasticized starch and organically modified montmorillonite (OMMT). The new materials were obtained by the technique of dynamic vulcanization and melt intercalation in a Plasti-Corder Brabender internal mixer, at 80 rpm and a temperature of 170°C. The influence of using the OMMT type nanofiller and the plasticized starch filler on the characteristics was observed. The new materials have a melt flow index of over 12g/10 min at 180°C for a force of 10 kg, which allows injection processing - an ecological method of processing polymeric materials. The samples show very good physical-mechanical characteristics both in the normal state and after accelerated aging at 168 hours at 170°C (tensile strength over 16 N/ mm2, tear strength over 102 N/mm, hardness 55-59°ShD, elasticity over 30%, etc.). The materials show high values of abrasion resistance (below 30 mm3), and very good results for mass and volume variation after 22 hours at 23°C in: water, acids and concentrated bases. These characteristics are due both to the composition of the new materials and to the obtaining technology. For evaluating the structural modification, analysis of the FT-IR spectral of the samples was carried out. The new materials can be used in different fields such as: in the footwear industry (soles, heels and plates), safety equipment (boots, etc), obtaining gaskets, hoses, technical rubber products for cars etc.
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Sonmez, Maria, Mircea Juganaru, Anton Ficai, Ovidiu Oprea, Roxana Trusca, Mihai Georgescu, Dana Gurau, et al. "Improvement of mechanical, thermal and morphostructural properties of SBS thermoplastic elastomer using kaolin and dolomite microparticles with modified surface." In The 8th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2020. http://dx.doi.org/10.24264/icams-2020.i.14.

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The aim of this paper was to assess the influence of the modification of the surface of dolomite and kaolin with SiO2 and TiO2 precursors, on the block copolymer styrene-butadiene-styrene (SBS) type thermoplastic rubber properties. These composite materials were obtained by compounding SBS with various ratio of powders. Based on the SEM images it can conclude that the powders were homogenously dispersed in to the SBS matrix. The dolomite particles can be clearly identified in the SEM images as particles of 10 micrometers. The samples obtained with modified dolomite have similar morphology. The EDS elemental distribution confirming a good corroboration between the elements of the dolomite, kaolin and titanium or silicon elements. Based on the thermal analysis according to the residual mass, the presence of 20% mineral phase can be confirmed. According to the DSC curves a strong stabilization of the composite appears, because of the presence of the mineral component. According to the physical-mechanical data all the composite materials exhibit improved mechanical properties. Additionally, the modification of the kaolin and/or dolomite bring important improvements in mechanical properties. The samples 13 and 14 exhibit high tensile and tear strength. These composites can be used for various applications, such as, for instance, soles for firefighters' footwear.
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