Soft Vulcanized Rubber. Effect of Temperature and Oxygen Pressure on Aging Rate

1937 ◽  
Vol 10 (2) ◽  
pp. 336-345
Author(s):  
J. H. Ingmanson ◽  
A. R. Kemp
Keyword(s):  
Oxygen Pressure ◽  
Mechanical Strain ◽  
Accelerated Aging ◽  
Effect Of Temperature ◽  
Aging Rate ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Cause Of Failure ◽  
Service Conditions ◽  
Oxidation Effect

Abstract IMPORTANT to the manufacturer and consumer of rubber goods are suitable accelerated aging tests for predicting readily the life of rubber articles under the variable storage and service conditions encountered. Since service conditions may involve the exposure of rubber to wide variations of temperature, light, and atmosphere under various types of mechanical strain, there is obviously need for a variety of tests, each designed to emphasize factors which are most important in any given set of service conditions. Since the primary cause of failure of soft vulcanized rubber in service is oxidation, emphasis has been placed on tests which accelerate the oxidation effect. The most widely adopted and generally satisfactory procedure of this type is the Bierer and Davis oxygen bomb method which involves heating the rubber under oxygen pressure. In Bierer and Davis' original publication (2), results were shown on the effect of increasing oxygen pressure in increments of 28.1 kg. up to 112.5 kg. per cm. on the aging of two different rubber compounds at the three temperatures, 50°, 60°, and 70° C. Their results showed that in some cases there was a uniform increase in aging rate with increased pressure and in other cases the rate increased rapidly up to a pressure of 28.7 kg. per sq. cm. but more slowly with further increases in pressure. In a later investigation (3) the same authors employed a pressure of 21.1 kg. per sq. cm. and 60° C. throughout. For the past ten years most laboratories have used an oxygen pressure of 21.1 kg. per sq. cm. and a temperature of 70° C., which may therefore be considered as standard.

Effect of Temperature and Pressure on Oxygen Pressure Aging

1943 ◽  
Vol 16 (2) ◽  
pp. 453-465 ◽  
Author(s):  
A. M. Neal ◽  
H. G. Bimmerman ◽  
J. R. Vincent
Keyword(s):  
Temperature Coefficient ◽  
Oxygen Pressure ◽  
The State ◽  
Effect Of Temperature ◽  
Individual Study ◽  
Aging Rate ◽  
Temperature Coefficients ◽  
Pressure Test ◽  
Temperature And Pressure

Abstract An increase in the temperature of the oxygen pressure test from 70° to 80° C greatly increases the rate of aging of rubber vulcanizates. The temperature coefficients of aging rate for the six stocks tested vary between 1.63 and 3.48. The state of cure markedly affects the temperature coefficient of some stocks. It is obvious that no change in the specification from 70° to 80° C should be made without first determining the temperature coefficient of the stock involved. A decrease in the pressure of the oxygen pressure test decreases the rate of aging, but the rate is not proportional to pressure. The relative rates of aging between 0.5 and 300 pounds oxygen pressure for the stocks tested vary between 1.09 and 4.87 for the normal cures, and between 1.50 and 6.74 for the longer cures. The state of cure markedly affects the change in rate of aging with change in pressure. The data show that changes in the pressure of the oxygen pressure test must be accompanied by a revision of all aging specifications, which will involve an individual study of each stock and every cure of each stock, since no correlation between stocks seems to exist for the changes in rate of aging that occur with changes in pressure.

Migration of Materials During Accelerated Aging By Oxygen Pressure Method

1951 ◽  
Vol 23 (11) ◽  
pp. 1646-1649 ◽  
Author(s):  
Marion Fackler ◽  
John Rugg
Keyword(s):  
Oxygen Pressure ◽  
Accelerated Aging ◽  
Pressure Method

Effect on Vulcanized Rubber Compounds of Immersion in Boiling Water

1931 ◽  
Vol 4 (3) ◽  
pp. 426-436
Author(s):  
K. J. Soule
Keyword(s):  
Water Absorption ◽  
Room Temperature ◽  
Anomalous Behavior ◽  
Boiling Water ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Different Temperatures ◽  
Actual Change

Abstract Further work is very desirable on the effect of different accelerators, antioxidants, and fluxes. It is possible that their study will throw more light on the mechanism of the swelling phenomena, and also help to explain the anomalous behavior of some of the fillers tested. It would also seem to be worth while to study the action of a few selected stocks in water, at several temperatures between room temperature and 100° C., to determine if the water absorption and swelling merely increase with rising temperatures, or whether there might be an actual change in behavior at different temperatures.

Performance of four plastics in relation to bolt relaxation in a non-conducting rail joint

1972 ◽  
Vol 7 (3) ◽  
pp. 194-204
Author(s):  
A S Mitchell ◽  
D Mills ◽  
R Kitching
Keyword(s):  
Cyclic Loading ◽  
Polymeric Materials ◽  
Electrical Insulation ◽  
Effect Of Temperature ◽  
Relaxation Behaviour ◽  
Static Tests ◽  
Service Conditions

Experiments have been conducted to observe the relaxation behaviour of fishplate-bolted rail joints in which four different polymeric materials were used for electrical insulation. Static tests were conducted to study the effect of temperature and of different locking sequences for the bolts on a rig which simulated service conditions at a joint. The effect of cyclic loading was considered.

Studies in the Vulcanization of Rubber. IV—A Theory of Vulcanization of Rubber

1930 ◽  
Vol 3 (4) ◽  
pp. 659-667
Author(s):  
G. R. Boggs ◽  
J. T. Blake
Keyword(s):  
Electrical Properties ◽  
Joule Effect ◽  
Vulcanized Rubber ◽  
Chemical Theory ◽  
Rubber Compounds ◽  
Kinetics Of ◽  
Kinetics Of Vulcanization

Abstract A new theory has been advanced which, it is believed, explains completely the various phenomena connected with the vulcanization of rubber. It is entirely a chemical theory based on the existence of two separate and distinct rubber compounds, soft vulcanized rubber and ebonite. The theory explains satisfactorily the aging of rubber, the variation in combined sulfur at optimum cure caused by acceleration, the kinetics of vulcanization, the characteristics of various vulcanizing agents, the thermochemistry of vulcanization, the electrical properties of rubber, the reclaiming of rubber, and the Joule effect. A brief review and discussion of the phenomena and past theories of vulcanization have also been given.

Crystallization of Vulcanized Rubber

1941 ◽  
Vol 14 (2) ◽  
pp. 347-355 ◽  
Author(s):  
Norman Bekkedahl ◽  
Lawrence A. Wood
Keyword(s):  
Practical Importance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Single Exception ◽  
Quantitative Results ◽  
The Subject ◽  
Low Sulfur Content ◽  
Low Sulfur

Abstract The formation of crystals at room temperature by stretching rubber, vulcanized or unvulcanized, has been the subject of considerable study. The crystallization of unstretched rubber at low temperatures is also well known, but with a single exception to be discussed later, the effect has commonly been considered to be limited to the unvulcanized material. In the present investigation, however, the crystallization of unstretched specimens of vulcanized rubber of low sulfur content has been accomplished. In commercial vulcanized rubber products, crystallization has not hitherto been recognized as a factor of practical importance. It is probably significant in cold climates, where some rubber products slowly undergo a great increase in rigidity and permanent set. Automobile traffic counters, for example, have been rendered inoperative by the hardening of the rubber tubing used with them. Laboratory tubing and other products made of a number of different commercial rubber compounds have become rigid after storage for some weeks in a refrigerator at about 0° C. Previous work on unvulcanized rubber showed that it can be crystallized at temperatures between + 10° and −40° C, the crystals melting in a range from about 6° to 16° C. Crystallization and fusion are accompanied by changes in volume, heat capacity, light absorption, birefringence, x-ray diffraction, and mechanical properties such as hardness. x-Ray diffraction and birefringence, of course, give the most direct evidence of crystalline structure, but in the present work change of volume, measured in a mercury-filled dilatometer, was chosen as the criterion of crystallization or fusion. Quantitative results are more easily obtained in this manner, and the experimental observations are simple. Furthermore, the method is well adapted to continuous observations over long periods of time, such as were found necessary in the present work.

Long-term Adhesion Studies of Polyimide to Inorganic and Metallic Layers

2012 ◽  
Vol 1466 ◽  
Author(s):  
Juan S. Ordonez ◽  
Christian Boehler ◽  
Martin Schuettler ◽  
Thomas Stieglitz
Keyword(s):  
Silicon Carbide ◽  
Accelerated Aging ◽  
Shear Tests ◽  
Adhesion Promoters ◽  
Intermediate Layers ◽  
Aging Conditions ◽  
Cause Of Failure ◽  
One Year ◽  
Inorganic Layers

ABSTRACTDelamination between thin-film metal and substrate is a major cause of failure in polyimide based neural microelectrode arrays. Chemical adhesion is the only way to establish a long-term bond that will allow two materials to stick to each other even in a wet environment, given that the materials do not deteriorate in the presence of water. This study assesses, by means of peel and shear tests, a long-term quantitative and comparative study of the adhesion of polyimide to various metallic and other inorganic layers of interest. Polyimide (BPDA-PPD) was cured on the layers, which involve platinum, gold and tungsten-titanium as commonly used implant metals and diamond-like carbon (DLC), silicon carbide (SiC), silicon dioxide (SiO2) and silicone nitride (SiN) as potential adhesion promoters to be used later as intermediate layers between metal and polyimide. The adhesion was observed over one year under accelerated-aging conditions by storing the specimens in 60°C saline (corresponding to 40000 hrs at 37°C). Only silicon carbide and amorphous carbon showed almost unaffected adhesion to polyimide over the testing period. No water intrusion at the interface was observed and the strong bond is almost fully maintained.

Strain Test for Evaluation of Rubber Compounds

1949 ◽  
Vol 22 (1) ◽  
pp. 201-211 ◽  
Author(s):  
Frank L. Roth ◽  
Robert D. Stiehler
Keyword(s):  
High Precision ◽  
Chemical Reaction ◽  
Strain Measurements ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Order Chemical Reaction ◽  
Strain Testing ◽  
Order Of Magnitude ◽  
Single Sheet ◽  
Uniform Treatment

Abstract Measurements of elongation of rubber vulcanizates at a fixed stress have been made with a precision much greater than can be obtained in the usual measurements of stress at a specified elongation. Such measurements form the basis of a strain test developed to characterize rubber vulcanizates in control and research testing. Statistical analyses show that the errors introduced in the actual strain measurements are negligible compared to those introduced by variations during compounding and curing, whereas the errors introduced by the usual measurements of stress at a specified elongation are of the same order of magnitude as those for compounding and curing. The high precision of strain testing has been used to detect variations within a single sheet of vulcanized rubber and variations among sheets cured from the same compounded batch. It has been possible also to determine with a single sheet its change in stiffness or modulus with age. The uniform treatment of specimens in the strain test makes them particularly useful for precise measurements of set. Further, it has been found that the decrease in elongation with time of cure apparently follows the laws of a second-order chemical reaction; consequently it is possible to represent the data by an equation involving three vulcanization parameters.

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