Effect of the network topology on the tensile strength of natural rubber vulcanizate at elevated temperature

2005 ◽  
Vol 98 (3) ◽  
pp. 1219-1223 ◽  
Author(s):  
L. González ◽  
J. L. Valentín ◽  
A. Fernández-Torres ◽  
A. Rodríguez ◽  
A. Marcos-Fernández
Keyword(s):  
Tensile Strength ◽  
Elevated Temperature ◽  
Natural Rubber ◽  
Network Topology ◽  
Rubber Vulcanizate

Tensile and Tear Behavior of Anisotropic Double Networks of a Black-Filled Natural Rubber Vulcanizate

1998 ◽  
Vol 71 (5) ◽  
pp. 846-860 ◽  
Author(s):  
G. R. Hamed ◽  
M. Y. Huang
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Stress Strain ◽  
Double Network ◽  
Extension Ratio ◽  
Rubber Vulcanizate ◽  
Double Networks ◽  
Strain Responses ◽  
Sheet Stretching ◽  
Weakly Dependent

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.

Measurement of Tensile Strength of Natural Rubber Vulcanizates at Elevated Temperature

1982 ◽  
Vol 55 (1) ◽  
pp. 66-75 ◽  
Author(s):  
C. L. M. Bell ◽  
D. Stinson ◽  
A. G. Thomas
Keyword(s):  
Tensile Strength ◽  
Elevated Temperature ◽  
Critical Temperature ◽  
Natural Rubber ◽  
Test Piece ◽  
Flaw Size ◽  
High Tensile Strength ◽  
Test Pieces ◽  
Naturally Occurring ◽  
Natural Rubber Vulcanizates

Abstract The tensile strength of test pieces made from natural rubber vulcanizates drops abruptly at a critical temperature which can vary from 40 to 130°C. This variation in critical temperature is shown here to be a result of the variation in critical cut length with temperature. When the naturally occurring flaws in the test piece are smaller than the critical cut length, high tensile strength values occur, but when the flaws are longer than the critical cut length, low tensile strength values occur. The critical cut length decreases as the temperature increases, and the abrupt drop in tensile strength occurs as the critical cut length reaches the natural flaw size in the test piece. The natural flaw size in tensile test pieces depends on the sharpness of the cutter, and for tensile strength measurements at elevated temperature, it is shown that even a slightly blunt cutter may give markedly different results from a sharp one.

Tensile Strength of Protein-free Natural Rubber and its Vulcanizate Soaked in Water

2020 ◽  
Vol 93 (9) ◽  
pp. 293-299
Author(s):  
Luu Thanh HUYEN ◽  
Chen Ao RAN ◽  
Yoshimasa YAMAMOTO ◽  
Seiichi KAWAHARA
Keyword(s):  
Tensile Strength ◽  
Natural Rubber

Pengaruh penambahan natural rubber (NR), epoxidation natural rubber (ENR-46) dan chlorprene rubber (CR) pada sifat kompon termoplastik

2020 ◽  
Vol 26 (2) ◽  
pp. 62-69
Author(s):  
Farida Ali ◽  
Tuti I. Sari ◽  
Andi A. Siahaan ◽  
Al-Kautsar D. Arya ◽  
Tri Susanto
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Vinyl Chloride ◽  
Butadiene Rubber ◽  
Elongation At Break ◽  
Nitrile Butadiene Rubber ◽  
Poly Vinyl Chloride

Penelitian ini untuk mengetahui pengaruh penambahan Natural Rubber (NR) dan Epoxidation Natural Rubber (ENR-46) dengan kompatibiliser Chlorprene Rubber (CR) pada aplikasi kompon termoplastik Poly Vinyl Chloride (PVC) dan Nitrile Butadiene Rubber (NBR), variabel penelitian meliputi ENR-46/PVC/NBR/CR, NR/PVC/NBR/CR dan CR-NR/PVC/NBR, CR-ENR-46/PVC/NBR. Parameter pengujian sifat fisik-mekanik : Hardness (Shore A), Tensile Strength (Mpa), Elongation at Break (%) dan ketahanan terhadap pelarut minyak (n-Pentane, Toluene, Hexane dan Pertalite). Hasil penelitian didapatkan untuk sifat fisik-mekanik, semakin banyak penambahan NR Kekerasan kompon termoplastik akan menurun, Tensile Strength dan Elongation at Break kompon akan meningkat begitu juga dengan CR-NR. Tetapi berbanding terbalik hasilnya untuk ENR-46 dan CR-ENR-46. Pengujian Ketahanan terhadap pelarut minyak semakin banyak penambahan ENR-46 Ketahanan kompon termoplastik terhadap pelarut akan meningkat, hasil yang sama juga pada CR-ENR-46. Tetapi berbanding terbalik hasilnya dengan penambahan NR dan CR-NR pada kompon termoplastik.

EFFECT OF ZINC DITHIOCARBAMATES AND THIAZOLE-BASED ACCELERATORS ON THE VULCANIZATION OF NATURAL RUBBER

2012 ◽  
Vol 85 (1) ◽  
pp. 120-131 ◽  
Author(s):  
Md. Najib Alam ◽  
Swapan Kumar Mandal ◽  
Subhas Chandra Debnath
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
High Performance Liquid Chromatography ◽  
Liquid Chromatography ◽  
Reaction Mechanism ◽  
Natural Rubber ◽  
High Performance ◽  
Binary Systems ◽  
Synergistic Activity ◽  
Tetramethylthiuram Disulfide

Abstract Several zinc dithiocarbamates (ZDCs) as accelerator derived from safe amine has been exclusively studied in the presence of thiazole-based accelerators to introduce safe dithiocarbamate in the vulcanization of natural rubber. Comparison has been made between conventional unsafe zinc dimethyldithiocarbamate (ZDMC) with safe novel ZDC combined with thizole-based accelerators in the light of mechanical properties. The study reveals that thiuram disulfide and 2-mercaptobenzothiazole (MBT) are always formed from the reaction either between ZDC and dibenzothiazyledisulfide (MBTS) or between ZDC and N-cyclohexyl-2-benzothiazole sulfenamide (CBS). It has been conclusively proved that MBT generated from MBTS or CBS reacts with ZDC and produces tetramethylthiuram disulfide. The observed synergistic activity has been discussed based on the cure and physical data and explained through the results based on high-performance liquid chromatography and a reaction mechanism. Synergistic activity is observed in all binary systems studied. The highest tensile strength is observed in the zinc (N-benzyl piperazino) dithiocarbamate-accelerated system at 3:6 mM ratios. In respect of tensile strength and modulus value, unsafe ZDMC can be successfully replaced by safe ZDCs in combination with thiazole group containing accelerator.

scholarly journals Biocomposites of Epoxidized Natural Rubber/Poly(lactic acid) Modified with Natural Fillers (Part I)

2021 ◽  
Vol 22 (6) ◽  
pp. 3150
Author(s):  
Anna Masek ◽  
Stefan Cichosz ◽  
Małgorzata Piotrowska
Keyword(s):  
Tensile Strength ◽  
Lactic Acid ◽  
Natural Rubber ◽  
Epoxidized Natural Rubber ◽  
Poly Lactic Acid ◽  
Uv Aging ◽  
High Elasticity ◽  
Natural Fillers ◽  
Natural Additives

The study aimed to prepare sustainable and degradable elastic blends of epoxidized natural rubber (ENR) with poly(lactic acid) (PLA) that were reinforced with flax fiber (FF) and montmorillonite (MMT), simultaneously filling the gap in the literature regarding the PLA-containing polymer blends filled with natural additives. The performed study reveals that FF incorporation into ENR/PLA blend may cause a significant improvement in tensile strength from (10 ± 1) MPa for the reference material to (19 ± 2) MPa for the fibers-filled blend. Additionally, it was found that MMT employment in the role of the filler might contribute to ENR/PLA plasticization and considerably promote the blend elongation up to 600%. This proves the successful creation of the unique and eco-friendly PLA-containing polymer blend exhibiting high elasticity. Moreover, thanks to the performed accelerated thermo-oxidative and ultraviolet (UV) aging, it was established that MMT incorporation may delay the degradation of ENR/PLA blends under the abovementioned conditions. Additionally, mold tests revealed that plant-derived fiber addition might highly enhance the ENR/PLA blend’s biodeterioration potential enabling faster and more efficient growth of microorganisms. Therefore, materials presented in this research may become competitive and eco-friendly alternatives to commonly utilized petro-based polymeric products.

scholarly journals Composites from Thermoplastic Natural Rubber Reinforced Rubberwood Sawdust: Effects of Sawdust Size and Content on Thermal, Physical, and Mechanical Properties

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Chatree Homkhiew ◽  
Surasit Rawangwong ◽  
Worapong Boonchouytan ◽  
Wiriya Thongruang ◽  
Thanate Ratanawilai
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Natural Rubber ◽  
High Density Polyethylene ◽  
High Performance ◽  
Physical And Mechanical Properties ◽  
Modulus Of Rupture ◽  
Shore Hardness ◽  
Thermoplastic Natural Rubber ◽  
Plastic Content

The aim of this work is to investigate the effects of rubberwood sawdust (RWS) size and content as well as the ratio of natural rubber (NR)/high-density polyethylene (HDPE) blend on properties of RWS reinforced thermoplastic natural rubber (TPNR) composites. The addition of RWS about 30–50 wt% improved the modulus of the rupture and tensile strength of TPNR composites blending with NR/HDPE ratios of 60/40 and 50/50. TPNR composites reinforced with RWS 80 mesh yielded better tensile strength and modulus of rupture than the composites with RWS 40 mesh. The TPNR/RWS composites with larger HDPE content gave higher tensile, flexural, and Shore hardness properties and thermal stability as well as lower water absorption. The TPNR/RWS composites with larger plastic content were therefore suggested for applications requiring high performance of thermal, physical, and mechanical properties.

Graft Polymers Derived from Natural Rubber

1956 ◽  
Vol 29 (1) ◽  
pp. 99-105 ◽  
Author(s):  
G. F. Bloomfield ◽  
F. M. Merrett ◽  
F. J. Popham ◽  
P. Mc L. Swift
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Methyl Methacrylate ◽  
Transfer Reaction ◽  
Polymer Chains ◽  
Vinyl Monomers ◽  
Grafted Polymer ◽  
Polymeric Chains ◽  
Graft Polymers ◽  
Direct Growth

Abstract Graft polymers result when vinyl monomers are polymerized in the presence of natural rubber, either in solution or as latex, and some of the polymeric chains become attached to the rubber molecules. The properties of the natural rubber can be widely modified according to the nature and the amount of the grafted polymer. The polymer-modified natural rubber appears to be produced by direct growth of polymer chains on to rubber molecules rather than by a transfer reaction involving the rubber. Graft polymers of styrene and methyl methacrylate with natural rubber can be compounded and cured to give light-colored articles of good tensile strength, and rubber-methyl methacrylate graft polymers have outstanding flex-cracking and fatigue resistance.

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