The Tear Resistance of Rubber Compounds

1941 ◽  
Vol 14 (4) ◽  
pp. 863-876
Author(s):  
G. A. Patrikeev ◽  
A. I. Melnikov

Abstract 1. An improved method of measuring tear resistance was developed. The samples which were examined were cut in the direction of stretching. 2. The relation between tear resistance and time of vulcanization was investigated. 3. The tear resistances of synthetic and natural rubbers were compared. 4. It is shown that the tear resistance of samples of natural and synthetic rubber depends on the depth of the initial cut. With short cuts, natural rubber has a higher tear resistance than synthetic rubber, but this difference decreases as the cut is made longer. 5. It is established that the tear resistance of thin rubber specimens is smaller than that of thicker specimens. 6. The mechanism of tear resistance is discussed. Factors such as deformation are considered.

2020 ◽  
Vol 276 ◽  
pp. 122933
Author(s):  
Xianjie Ren ◽  
Cindy S. Barrera ◽  
Janice L. Tardiff ◽  
Andres Gil ◽  
Katrina Cornish

1957 ◽  
Vol 30 (2) ◽  
pp. 639-651 ◽  
Author(s):  
I. Sagajllo

Abstract Important claims have been made in recent years regarding the capacity of lignin to reinforce natural and synthetic rubber. In 1949 Dawson reviewed the literature on the use of lignin in rubber and drew particular attention to the work of Keilen and Pollak who had shown that in certain circumstances lignin could be considered to rival EPC black in its ability to yield strong GR-S vulcanizates with high resistance to tear. Raff and his coworkers subsequently showed that the reinforcement of GR-S by lignin is enhanced if the lignin, before coprecipitation with the latex, is subjected to oxidation; other workers studied the application of lignin to the reinforcement of different elastomers, the influence of coprecipitation conditions on the properties of the product, and the problem of overcoming the delaying effect of lignin on vulcanization of lignin-natural rubber coprecipitates. Keilen and Pollak in their experiments incorporated lignin into rubber by coprecipitation at the latex stage, but they indicated that similar results could be obtained if lignin “in the gelled state” was added to rubber by milling. No reinforcement was observed however when lignin was added to rubber as a dry powder. Lignin is potentially an abundant and cheap material which according to the above claims should extend the range of useful compounds available to rubber manufacturers. The present paper describes work undertaken to gain firsthand knowledge of the technique of coprecipitating lignin with natural rubber from preserved latex, to learn something about the properties of natural rubber compounds prepared from lignin coprecipitates, and to study possible ways of incorporating lignin into rubber by means other than coprecipitation. It also records test results for masterbatches prepared by the Rubber Research Institute of Malaya from fresh latex on a pilot plant scale.


1941 ◽  
Vol 14 (4) ◽  
pp. 786-798
Author(s):  
A. Kusov

Abstract 1. A method of measuring the tear resistance of rubber compounds was developed. This method has a number of advantages over other methods (Goodrich, Heidensohn, Goodyear, etc.), including the following. (a) The symmetrical shape and the large surface of tearing (20 sq. cm.). This excludes the possibility of short, accidental tears, and enables better observation of the nature of the tear. (b) Owing to the small size of the clamped portion of the specimen compared to the size of the tearing surface, “end effects” are largely eliminated. (c) Tearing forces are registered periodically (every 10 seconds), and it is possible in this way to determine the total energy expended on tearing, and the nature of its changes. (d) The experiments are easy to perform, and the apparatus is simple. 2. The addition of carbon black (10–100 per cent) to synthetic rubber compounds increases considerably the tear resistances of the vulcanized products. The best results are obtained with compounds containing between 50 and 75 per cent of carbon black. 3. A zinc oxide content of between 8 and 14 per cent improves the tear resistances of compounds of both synthetic and natural rubbers. 4. Compounds with increased fibrous structure show increased abrasion resistance when the fiber direction is parallel to the movement of the abrading surface. 5. Compounds cured for short times only show low tear resistances when made of synthetic rubbers of both low (0.31) and high (0.87) plasticity. The best results are obtained with compounds made of synthetic rubber of medium plasticity (0.53 and 0.40) (see Figure 4). 6. When comparing tear resistances, it is of the utmost importance to maintain the thickness of test-specimens within narrow limits. It is desirable to keep variations within 10–15 per cent. 7. The weakening of the uncut portion of a test-specimen with increase in depth of cut is less pronounced with compounds of synthetic rubber than it is with natural rubber compounds, particularly in the case of overcured samples. With synthetic compounds, this weakening effect varies 2–3 times; with natural rubber compounds it is 3.5–6.5 times. The relation between tear resistance and depth of cut is shown in Figure 5 and Table VI. 8. Carbon black compounds of both synthetic and natural rubbers exhibit various structural forms of tearing. Synthetic rubber compounds with low tear resistances show simple and smooth tearing surfaces, usually in the prolongation of the cut, or at a slight angle to it (Figure 1, type A or intermediate between A and B). Synthetic compounds with high tear resistances show complicated tearing surfaces (Figures 6 and 7, types C, D, E and F).


2012 ◽  
Vol 78 (13) ◽  
pp. 4543-4551 ◽  
Author(s):  
Meral Yikmis ◽  
Alexander Steinbüchel

ABSTRACTThis review intends to provide an overview of historical and recent achievements in studies of microbial degradation of natural and synthetic rubber. The main scientific focus is on the key enzymes latex-clearing protein (Lcp) from the Gram-positiveStreptomycessp. strain K30 and rubber oxygenase A (RoxA) from the Gram-negativeXanthomonassp. strain 35Y, which has been hitherto the only known rubber-degrading bacterium that does not belong to the actinomycetes. We also emphasize the importance of knowledge of biodegradation in industrial and environmental biotechnology for waste natural rubber disposal.


1929 ◽  
Vol 2 (3) ◽  
pp. 441-451 ◽  
Author(s):  
Thomas Midgley ◽  
Albert L. Henne

Abstract Two hundred pounds of pale crepe rubber have been destructively-distilled at atmospheric pressure. The distillate was fractionated and its components identified from C5 to C10, as shown in the table. Assuming that the Staudinger formula is correct, that the single bonds furthest from the double bonds are the weaker spots and that the formation of six-carbon rings is favored, it has been shown that nearly all of the compounds actually isolated could be predicted. The experimental results, together with forthcoming experimental data, are expected to be used to throw light upon the formula of the rubber molecule.


1951 ◽  
Vol 24 (2) ◽  
pp. 436-446 ◽  
Author(s):  
G. Salomon ◽  
C. Koningsberger

Abstract A number of hydrochlorides of natural and synthetic rubbers and allied polymers have been prepared and subjected to kinetic analysis with organic bases. The hydrochlorides of natural rubber react at 100° C at a rate identical to that of low-molecular tertiary chlorides. At 50° C the reactivity of the polymer is, however, reduced by physical factors. The hydrochloride of GR-S (a synthetic rubber made from butadiene and styrene) has been prepared for the first time by heating the swollen polymer with HC1 under pressure. Kinetic analysis of this product revealed two fractions: the expected secondary chloride, and a small fraction of a very reactive (tertiary?) chloride. After elimination of experimental difficulties, we succeeded in the preparation and kinetic identification of the pure tertiary hydrobromide of natural rubber. Attempts to prepare the secondary bromide under peroxide conditions failed. Kinetic analysis of two types of Neoprene revealed the presence of a small quantity of allylic groups in the polymer, while 95 per cent of the chlorine in Neoprene has the expected stability of a vinyl chloride. This stability can be used for the identification of Neoprene.


2013 ◽  
Vol 812 ◽  
pp. 93-99
Author(s):  
N.H.H. Shuhaimi ◽  
Nadras Othman ◽  
Hanafi Ismail ◽  
S. Sasidharan

Effect of natural and synthetic antioxidants on curing characteristic and properties of different natural rubber (NR) origin compounds were performed in this study. The evaluations of natural antioxidant (NA) performance in different NR origins were conducted and the changes in curing characteristic, crosslink density, fatigue life and compression set were recorded. The results indicated that Standard Thailand Rubber (STR) compound has longer processing time in curing characteristic due to a longer chain which is high molecular weight. Because of that, crosslink density, fatigue life cycle (Kc) and compression set (%) of STR compound show better result compared to other origins. On the other hand, NR compounds with NA have show better fatigue and compression set compared with trimethylquinoline (TMQ) especially for STR 5L. Thus, NA can be used as an alternative to the commercial antioxidant in all rubber compounds.


1953 ◽  
Vol 26 (2) ◽  
pp. 336-349
Author(s):  
J. R. Beatty ◽  
A. E. Juve

Abstract The practical implications of this study are that rubber compounds which swell in the presence of oil have a property which may be utilized in some applications where it may serve a useful purpose. Examples are O-ring seals and other types of gaskets, where the rubber is used in compression. In these cases the stress decays more slowly with time, and in some cases the force would increase, and the tendency to leakage would be minimized. In these experiments the sample was relatively unconfined except for the direction of loading with only low frictional forces which tended to prevent increase in volume. It was noted (Figures 4 and 6) that, with natural rubber and GR-S at 70° C the stress reached a maximum between 1000 and 10,000 hours, which is a result of the sample reaching equilibrium with respect to swelling by the oil, and the stress then decreases, depending on the oxidative scission of bonds in the same manner as found for tests conducted in air. However, according to Scott, the attack of swelling agents accelerates oxidation; so it is possible that this oxidative scission might be in addition to that normally measured in air.


1936 ◽  
Vol 9 (1) ◽  
pp. 74-82
Author(s):  
Thomas Midgley ◽  
A. L. Henne ◽  
A. F. Shepard ◽  
Mary W. Renoll

Abstract It has been shown that natural rubber conthins oxygen, while synthetic rubber is oxygen free. This oxygen appears to be of an hydroxylic type, and its quantity corresponds to about one hydroxyl group for each one thousand isoprene units of the rubber molecule. Rubber has been allowed to oxidize and a mechanism is proposed to interpret the quantitative data recorded.


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