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

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.

1969 ◽  
Vol 42 (5) ◽  
pp. 1412-1419
Author(s):  
J. Lal

Abstract The chemical nature of crosslinks in natural rubber—sulfur—diphenylguanidine vulcanizates was modified by reaction with triphenylphosphine under nitrogen to determine the effect of this change on tensile strength and oxygen absorption characteristics of the vulcanizates. The vulcanizates were characterized by organically combined sulfur and polysulfidic sulfur. Polysulfidic crosslinks, i.e., crosslinks containing three or more sulfur atoms in the crosslink, were found not to be essential for the attainment of high tensile strength in these vulcanizates. Data for the samples which had lost significant amounts of polysulfidic crosslinks by reaction with triphenylphosphine fitted the tensile strength versus 300% modulus curve for the control samples. Vulcanizates which had been reacted with triphenylphosphine for 16 days at 80° C, had lost 95–99.6% of their polysulfidic sulfur. These triphenylphosphine-reacted vulcanizates exhibited significantly lower rates of oxygen absorption at 100° C as compared to the untreated vulcanizates. This suggests that polysulfidic structures in the original vulcanizates act as oxidation initiators.


1966 ◽  
Vol 39 (3) ◽  
pp. 755-762
Author(s):  
S. N. Angove ◽  
E. S. Graham ◽  
G. Hilditch ◽  
R. A. Stewart ◽  
F. L. White

Abstract Foam rubber properties have been measured for NIR latexes as a function of acrylonitrile content of the copolymer and as a function of ratio of NIR latex to NR latex and high modulus SBR latex. Foam rubber made from NIR latex had good aging and oil resistance, combined with the desirable high tensile strength and elongation characteristic of natural rubber foam. Resilience and low temperature flexibility of NIR foams were found to be lower than that achieved with foams of either SBR or NR latexes. Although compression modulus of NIR foam was lower than that of a high modulus SBR foam and approximately equivalent to that of NR foam, it was effectively increased by the addition of either such SBR latex or a high-styrene resin latex.


2016 ◽  
Vol 705 ◽  
pp. 35-39 ◽  
Author(s):  
Bryan B. Pajarito ◽  
Jimyl Arabit

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).


2002 ◽  
Vol 75 (5) ◽  
pp. 935-942 ◽  
Author(s):  
G. R. Hamed ◽  
N. Rattanasom

Abstract Tensile strengths, σb, of gum and N115-filled natural rubber test pieces, with and without edge pre-cuts, have been determined. At low crosslink density, the regular (uncut) σb of filled and gum vulcanizates is similar. However, at high crosslink density, the gum NR becomes brittle, while the corresponding filled rubber remains strong and resistant to cut growth. It is proposed that the tightly linked gum does not strain-crystallize appreciably during stretching, but that its filled counterpart does. Carbon black appears capable of inducing crystallization in a network that alone remains amorphous during extension. Filled vulcanizates of various crosslink densities have similar normal tensile strengths ( ≈ 30 MPa), but strengths differ, sometimes more than twofold, if a pre-cut is present. Lightly crosslinked specimens containing a small cut have strengths that depend very weakly on cut size, c. Furthermore, these develop long longitudinal cracks from which catastrophic rupture initiates. With larger cuts, strength decreases more rapidly with increasing c, there is less longitudinal crack growth, and rupture initiates near the original cut tip. In contrast, the strength of a highly crosslinked vulcanizate is sensitive to small cuts and test pieces exhibit minimal longitudinal cracking before failure.


1959 ◽  
Vol 32 (2) ◽  
pp. 477-489 ◽  
Author(s):  
A. G. Thomas

Abstract It has been noted in Part I of this series (referred to hereafter as I), that if a nicked specimen of a natural rubber vulcanizate is slowly stretched, tearing occurs at the tip for quite small applied forces. In the initial stages, this tearing continues only as long as the deformation of the specimen is being increased, and virtually ceases if the deformation is held constant. This tearing is essentially time independent, and is termed “static” cut growth. If, however, the deformation is continued until the cut has grown by a few hundredths of a millimeter the growth becomes time dependent and catastrophic tearing takes place, the cut suddenly increasing in length by perhaps a millimeter or so. If a nicked specimen is alternately stretched and relaxed to the unstrained state, the cut gradually grows even though the applied force is less than that required to produce catastrophic tearing. This phenomenon is termed “dynamic” cut growth. This behavior can be compared to that of gum GR-S vulcanizates described in Part III, where static cut growth of the above type does not occur, a dead load on a test piece producing a more or less steady rate of cut growth. In the present paper, measurements on natural rubber gum vulcanizates only are described, and the numerical results expressed in terms of the theory developed in previous papers (Parts I, II and III). It has been shown in I and II that the tear behavior of differently shaped test pieces cut from thin sheets of thickness t may be correlated by means of the concept of the energy for tearing. This is defined as the value of T[=(1/t)(∂W/∂c)l] at the instant of tear, and is denoted by Tc. In the definition of T, is the total elastic energy stored in the test piece, c the length of the cut, and the subscript l indicates that the differentiation is to be carried out at constant displacement of those parts of the boundary that are not force-free. It was also shown that a convenient and direct method of obtaining Tc is by the use of the “simple extension” tear test piece described in I and shown in Figure 1, and this has been used for most of the experiments. Under most conditions, T for this test piece is nearly independent of the cut length, width of the test piece, and modulus of the rubber; T is very nearly equal to 2F/twhere F is the force applied to the arms. In the cases where the use of the above approximate relation between T and F introduces an appreciable error, the exact theory given in I was used.


1970 ◽  
Vol 43 (2) ◽  
pp. 222-228 ◽  
Author(s):  
A. G. Thomas ◽  
J. M. Whittle

Abstract The dependence of tensile strength of a number of vulcanizates on temperature has heen studied. A critical temperature θc is found for natural rubber at which an abrupt change in strength occurs. This temperature depends on degree of crosslinking and also on the nature of the vulcanizing system. The presence of carbon black filler increases the strength above θc but has little influence on the value of θc or the strength at temperatures below it. The behavior can be explained qualitatively in terms of a change in mechanism of rupture from essentially a tear process above θc to a crack growth process below it. The influence of vulcanizing system is mainly due to changes in the nature of the crosslink rather than changes in regularity of the main chain as shown by the rate of low temperature crystallization.


2011 ◽  
Vol 84 (2) ◽  
pp. 229-242 ◽  
Author(s):  
Gary R. Hamed ◽  
Kanoktip Boonkerd

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.


1959 ◽  
Vol 32 (2) ◽  
pp. 614-627 ◽  
Author(s):  
J. N. Short ◽  
G. Kraus ◽  
R. P. Zelinski ◽  
F. E. Naylor

Abstract The physical properties of polybutadiene vulcanizates have been measured as a function of polymer microstructure. Although the over-all properties of any one polybutadiene are determined by the relative ratio of cis, trans and vinyl units in the polymer chain, marked changes in physical properties do not occur until a relatively pure configuration is approached or unless the raw polymer displays crystallinity. Thus, polybutadienes containing more than 85 per cent cis, trans or vinyl units are characteristically different from each other and the differences are accentuated as the isomeric forms approach 100 per cent of a given configuration. Polybutadiene of 95 per cent cis configuration displays very low heat generation and high resilience (equaling natural rubber in these properties) and excellent abrasion resistance. trans-Polybutadiene (90 per cent), a crystalline plastic in the raw state, becomes rubbery after vulcanization. Gum vulcanizates possess high tensile strength, and tread stocks display high modulus and tensile strength, high hardness and fair hysteresis properties. Vulcanizates of amorphous 94 per cent vinyl polybutadiene are characterized by fair tensile properties, low hysteresis, and poor low temperature properties. Crystalline syndiotactic polybutadiene, 70 per cent vinly, displays much higher gum and tread tensile strengths than its amorphous counterpart. Amorphous polybutadienes containing less than 70–80 per cent of any one configuration are generally similar in most properties, and resemble emulsion polybutadiene in many respects. The wide range of properties of the various polybutadienes makes them suitable for many applications. cis-Polybutadiene is an excellent tire rubber, which has given as much as 40 per cent greater abrasion resistance than natural rubber in passenger tire tests. Heavy duty 10:00 × 20 truck tires fabricated with a 1:1 blend of cis-polybutadiene and natural rubber in the treads have given slightly better abrasion ratings and lower running temperatures than control tires fabricated entirely from natural rubber. Amorphous 80 per cent cis-polybutadiene has been found to possess exceptionally good low temperature properties, far superior to present arctic-type unsaturated elastomers, trans-Polybutadienes by virtue of their high modulus, high tensile strength, and high hardness could be utilized in the preparation of hard rubber goods, floor tiles, and shoe soles. While none of these polybutadienes is yet available commercially, their unusual properties and potential applicability in many areas should lead to their manufacture in the future.


2012 ◽  
Vol 488-489 ◽  
pp. 211-215 ◽  
Author(s):  
Pairote Klinpituksa ◽  
Sittaporn Somkieowan ◽  
Wae Asae Waehamad ◽  
Natinee Lopattananon

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.


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