Investigation of the Role of Intermolecular Forces in the Mechanism of High-Elastic Deformation. VII. The Effect of Molecular Interaction on the Fatigue Resistance of High Polymers Having Highly Developed Spatial Structures

1954 ◽  
Vol 27 (2) ◽  
pp. 363-373
Author(s):  
V. E. Gul ◽  
D. L. Fedyukin ◽  
B. A. Dogadkin
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Fatigue Resistance ◽  
Dibutyl Phthalate ◽  
Intermolecular Forces ◽  
Spatial Structures ◽  
Paraffin Oil ◽  
Degree Of Swelling ◽  
Natural Rubber Vulcanizates

Abstract It is shown experimentally that an irregular change of the fatigue resistance of loaded natural-rubber vulcanizates with increase of the degree of swelling in paraffin oil and in dibutyl phthalate is caused by the superposition of two processes: the increase of fatigue resistance, as a result of the reduction of mechanical losses, and the decrease of fatigue resistance due to the decrease of tensile strength proportional to the higher degree of swelling.

Changes of Fatigue Resistance of Vulcanized Natural Rubbers during Swelling

1953 ◽  
Vol 26 (1) ◽  
pp. 70-77 ◽  
Author(s):  
V. E. Gul ◽  
T. V. Dorokhina ◽  
B. A. Dogadkin
Keyword(s):  
Energy Loss ◽  
Natural Rubber ◽  
Fatigue Resistance ◽  
Modulus Of Elasticity ◽  
Dibutyl Phthalate ◽  
Relative Elongation ◽  
Chemical Processes ◽  
Initial Increase ◽  
Degree Of Swelling ◽  
Swollen Vulcanizates

Abstract A method of fatiguing swollen vulcanizates of natural rubber while maintaining a minimum deforming load, independent of the change of modulus of elasticity of the experimental specimens, was devised. The effect of swelling vulcanized natural rubber in petrolatum and in dibutyl phthalate on fatigue resistance was studied. With increase of swelling of a vulcanizate in dibutyl phthalate and in petrolatum, an initial increase of fatigue resistance was observed up to 1.8 times the fatigue resistance of the unswollen vulcanizate. Following this, a decrease of fatigue resistance was observed. The equation obtained for the change of fatigue resistance as a function of the degree of swelling is explained by two simultaneous processes: (1) increase of fatigue resistance because of decrease of energy loss in the destructionof intermolecular bonds, and (2) initiation of chemical processes leading to destruction, and a smaller difference between the deformation and the relative elongation at rupture. The effect of the character of the solvent used for swelling on the nature of the fatigue resistance-swelling relation is shown.

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.

Correlation of Blooming and Tensile Properties in Surfactant-Loaded Natural Rubber Vulcanizates

2016 ◽  
Vol 705 ◽  
pp. 35-39 ◽  
Author(s):  
Bryan B. Pajarito ◽  
Jimyl Arabit
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Tensile Properties ◽  
Tensile Strain ◽  
Tensile Modulus ◽  
Adhesive Tape ◽  
Taguchi Design Of Experiment ◽  
Convection Oven ◽  
Maximum Tensile Strain ◽  
Natural Rubber Vulcanizates

Tensile properties of surfactant-loaded natural rubber (NR) vulcanizates are investigated in correlation with blooming. Rubber sheets are compounded using an L12 orthogonal array of Taguchi design of experiment, where ingredients are treated as factors varied at low and high loadings. Blooming experiments are carried out by placing NR sheets in a natural convection oven set at 50 °C for 20 days. The amount of bloom on the surface is removed using adhesive tape and is monitored with time. Tensile properties of rubber dogbone samples are also measured with time. Results show that 5 out of 12 formulations show blooming to be significantly related to tensile modulus (0.005 < p < 0.039). It is observed that the tensile modulus increases with blooming (0.898 < r < 0.973). Three formulations indicate significant correlation of blooming with tensile strength (0.022 < p < 0.047). As observed, tensile strength decreases with blooming (-0.884 < r < -0.930). Five formulations signify blooming to have significant correlation with maximum tensile strain (0.000 < p < 0.011), which decreases with blooming (-0.957 < r < -0.995). Two formulations imply significant negative (-0.960 < r < -0.963) correlation between blooming and tensile set (p= 0.009).

EFFECT OF CURE EFFICIENCY ON PROPERTIES OF GUM AND BLACK FILLED NATURAL RUBBER VULCANIZATES

2011 ◽  
Vol 84 (2) ◽  
pp. 229-242 ◽  
Author(s):  
Gary R. Hamed ◽  
Kanoktip Boonkerd
Keyword(s):  
Electron Microscopy ◽  
Tensile Strength ◽  
Natural Rubber ◽  
Crosslink Density ◽  
Cure Time ◽  
Cracking Pattern ◽  
Natural Rubber Vulcanizates ◽  
Scanning Electron ◽  
Fracture Specimens ◽  
Strength Effect

Abstract Effects of the sulfur cure efficiency on the reversion behavior and the normal and edge-cut tensile strength of gum and black filled natural rubber (NR) vulcanizates were studied. N, N-dicyclohexyl-2-benzothiazole sulfenamide (DCBS) was used as an accelerator. A series of five vulcanizates with high to low cure efficiencies was prepared by increasing the sulfur (S) to DCBS ratios within the range of 0.26–6.66. All vulcanizates were formulated to have the same crosslink density. The degree of reversion (%) calculated from cure curves of gum and black filled NR at 20 min above the cure time (tc100) passed through maximum with decreasing cure efficiencies. For both gum and black filled NR, the highest degree of reversion (%) was observed at the S/DCBS ratio of 1.17. The normal tensile strengths of gum and black filled NR were directly proportional to the cure efficiency. For gum NR vulcanizates, the edge-cut tensile strength was markedly influenced by cure efficiency. Similar to the normal tensile strength, the gum NR vulcanizates cured with the lowest cure efficiency showed the lowest edge-cut tensile strength. Effect of the cure efficiency on the edge-cut tensile strength was less in the case of black filled NR vulcanizates. However, the black filled NR vulcanizates cured with the lowest cure efficiency also showed the lowest edge-cut tensile strength. The cut tip characteristics of the fracture specimens were investigated using scanning electron microscopy. The gum specimens showed only the simple lateral cracking pattern, while all black filled specimens showed the longitudinal cracking pattern. Four different cracking patterns of the black filled specimens were identified. The distribution of cracking patterns depended strongly on the size of precut and the cure efficiency.

Polymeric Antioxidant Based on Natural Rubber Grafted with N-(4-Hydroxyphenyl)maleimide

2012 ◽  
Vol 488-489 ◽  
pp. 211-215 ◽  
Author(s):  
Pairote Klinpituksa ◽  
Sittaporn Somkieowan ◽  
Wae Asae Waehamad ◽  
Natinee Lopattananon
Keyword(s):  
Tensile Strength ◽  
Maleic Anhydride ◽  
Natural Rubber ◽  
Ftir Spectroscopy ◽  
Accelerated Aging ◽  
Elongation At Break ◽  
Optimal Amount ◽  
Melt Grafting ◽  
Natural Rubber Vulcanizates

A novel rubber bound antioxidant NR-g-HPM was prepared by melt grafting HPM (N-(4-hydroxyphenyl)maleimide) onto natural rubber in a brabender plasticorder. HPM was synthesized from p-aminophenol and maleic anhydride. The yield was found to be over 80%. The grafting products were observed with FTIR spectroscopy and TGA. The ageing resistance of natural rubber vulcanizates using NR-g-HPM was studied. It was found that an optimal amount of NR-g-HPM (6 phr) gave about 25% better tensile strength and elongation at break as compared with conventional BHT addition, for filled natural rubber after 48 h of accelerated aging.

Effect of Epoxidized Oil on Tensile and Tear Strength of NR Vulcanizate and its Comparison with Aromatic Oil NR Vulcanizates

2013 ◽  
Vol 812 ◽  
pp. 204-209 ◽  
Author(s):  
Mohamed Rahmah ◽  
Wan Zain Norazira ◽  
Ahmad Faiza Mohd ◽  
Mohd Nurazzi Norizan
Keyword(s):  
Tensile Strength ◽  
Natural Rubber ◽  
Rubber Compound ◽  
Tear Strength ◽  
Green Component ◽  
Strength Tests ◽  
Tearing Energy ◽  
Polymer Industry ◽  
Natural Rubber Vulcanizates

Epoxidized oil (EO) is a sustainable oil that can be obtained form edible or non-edible naturals oil. The incorporation of epoxidized oil can increase the green component in rubber compound. It can contributes to worldwide technology specially in green tyre manufacturing. Epoxidized oil has the potential to replace aromatic oil (AO) to rubber and polymer industry. The effect of incorporation of EO and AO into natural rubber vulcanizates (NR) was studied via tensile and tear strength tests according to ISO 31-1977 and ISO 6133, respectively. Tensile strength of AO value showed greather value compared to EO. Gradual increases of elongation were observed form both AO and EO. Both moduli at 100% and 300% elongation, showed reductions as oil loading were increased. The tear strength results showed that tearing energy insignificantly increased with oil loading. EO compound was found to possess higher tearing energy compared to AO compound for most composition except for 15 pphr EO.

CURE CHARACTERISTICS OF DEVULCANIZED RUBBER:THE ISSUE OF LOW SCORCH

2017 ◽  
Vol 90 (3) ◽  
pp. 536-549 ◽  
Author(s):  
Anu Mary Joseph ◽  
Benny George ◽  
K. N. Madhusoodanan ◽  
Rosamma Alex
Keyword(s):  
Solvent Extraction ◽  
Natural Rubber ◽  
Main Chain ◽  
Process Safety ◽  
Original Sample ◽  
Vulcanized Rubber ◽  
Sulfur Vulcanization ◽  
Natural Rubber Vulcanizates ◽  
Devulcanized Rubber

ABSTRACT We investigate the reasons behind the observed low scorch during the revulcanization of devulcanized rubber. Mechanically devulcanized carbon black filled natural rubber vulcanizates originally cured by conventional vulcanization (CV), semiefficient vulcanization (semi EV), efficient vulcanization (EV), and peroxide systems as well as buffing dust obtained from pre-cured tread with known formulation were used. Revulcanization of these devulcanized samples using sulfur/sulfonamide system led to the following observations; irrespective of the type of sulfur cure system used for the initial vulcanization of the rubber, (i) the devulcanized samples cured without pre-vulcanization induction time and (ii) devulcanized samples prepared from peroxide vulcanized rubber cured with scorch safety. Based on the earlier reports that solvent extraction of devulcanized rubber did not improve the scorch time during revulcanization, the role of zinc bound non-extractable moieties was investigated using devulcanized rubber prepared from activator-free vulcanizates, which disproved the role of such moieties. This confirmed that the scorch reducing moieties should be attached to the rubber main chain, which can be unreacted crosslink precursors and cyclic sulfides left after the initial accelerated sulfur vulcanization of the original sample. The ability of pre-vulcanization inhibitor to induce scorch safety when devulcanized rubber is revulcanized as such, without adding any virgin rubber, proved that mercaptobenzothiazole (MBT) generated from crosslink precursors is the cause of low scorch. Acetone extracted devulcanized rubber samples prepared from tetramethyl thiuramdisulfide (TMTD) cured natural rubber, which does not follow the MBT pathway when revulcanized, cured with scorch safety, which further proved the role of MBT. Based on the previous reports and our results, it is obvious that powdering of rubber vulcanizate and devulcanization processes have no role on the low process safety of these materials, but it is inherent to the initial accelerated sulfur vulcanization chemistry undergone by these materials.

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