Low compression set butadine/acrylonitrile vulcanized rubber compounds

1960 ◽  
1931 ◽  
Vol 4 (3) ◽  
pp. 426-436
Author(s):  
K. J. Soule

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.


2009 ◽  
Vol 25 (2) ◽  
pp. 113-128 ◽  
Author(s):  
P. Raju ◽  
V. Nandanan ◽  
Sunil K.N. Kutty

Mechanical properties and the thermal degradation characteristics of natural rubber compounds with calophyllum inophyllum oil were compared to that of the control compound containing naphthenic oil. The compounds containing calophyllum inophyllum oil showed improved tensile strength, tear strength, modulus, compression set, abrasion resistance and resilience. Cure time was higher than the naphthenic oil mixes. Thermal studies showed an increase of 8 °C in the temperature of initiation of degradation and an increase of 6 °C in temperature at which the peak rate of degradation occurred. The peak rate of degradation was comparable to the control mix containing naphthenic oil.


2009 ◽  
Vol 30 (5) ◽  
pp. 1561-1568 ◽  
Author(s):  
A. Mostafa ◽  
A. Abouel-Kasem ◽  
M.R. Bayoumi ◽  
M.G. El-Sebaie

1930 ◽  
Vol 3 (4) ◽  
pp. 659-667
Author(s):  
G. R. Boggs ◽  
J. T. Blake

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.


1941 ◽  
Vol 14 (2) ◽  
pp. 347-355 ◽  
Author(s):  
Norman Bekkedahl ◽  
Lawrence A. Wood

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.


2021 ◽  
pp. 009524432110386
Author(s):  
Mousumi De Sarkar ◽  
Takashi Sunada ◽  
Atsunori Kondo

The curing system plays a vital role in designing rubber compounds for various industrial applications. Therefore, it is paramount to establish viable curing strategies for any new elastomer to explore its application potentials and commercial significance. Impacts of different curing regimes on the properties of a recently developed copolymer of chloroprene and acrylonitrile (acrylonitrile-chloroprene rubber, NCR) are reported here. Several primary accelerators (four from thiourea- and one from thiazolene product families) were used for curing the new rubber along with fixed loadings of zinc oxide (5 phr) and magnesium oxide (4 phr). Besides, curatives based on sulfur and peroxide were also evaluated. The influence of different curing systems on the rheological and physical properties of the copolymer was explored. It has been seen that the properties of the copolymer are considerably influenced by the different curing systems used. While ethylene thiourea (ETU) and propylene thiourea (PTU), as primary accelerators, provide the highest state of cure but may cause scorch. The use of trimethyl thiourea (TMU), on the other hand, results in the fastest rate and the most stable state of cure, good scorch safety, bin stability, and an overall good balance of properties. The sulfur-based crosslinking system induces good mechanical properties but causes limited bin stability, poor high-temperature compression set, and impaired heat resistance properties. As a curing agent, peroxide delivers the best bin stability in the rubber stocks but yields higher stiffness and limited aging resistance in the vulcanizates.


1949 ◽  
Vol 22 (1) ◽  
pp. 201-211 ◽  
Author(s):  
Frank L. Roth ◽  
Robert D. Stiehler

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.


2009 ◽  
Vol 79-82 ◽  
pp. 2171-2174 ◽  
Author(s):  
Chanchai Thongpin ◽  
C. Sangnil ◽  
P. Suerkong ◽  
A. Pongpilaiprertti ◽  
Narongrit Sombatsompop

This research is concentrated on the effect of concentration of silane-69 used for surface modification on precipitated silica (PSi), on cure characteristic and mechanical properties of PSi filled NR. The PSi content in this study was fixed at 20 phr in order to reveal the effect of silane used to modify PSi, on NR compound and vulcanizate. Moving Die Rheometer (MDR) was used to characterize cure characteristic of rubber compounds. Generally, scorch and cure time of NR would increase with the addition of PSi due to the absorption of accelerator on its surface whereas the addition of Si-69 modified PSi would reduce both scorch and cure time. It was found in this research that the excess amount of Si-69 used increased scorch and cure time of rubber compounds. This was thought to be that the excess of Si-69 led to the formation of polysiloxane clusters which could absorb accelerator in rubber compound and resulted in a prolonged scorch and cure time. In term of vulcanized rubber, it was found that maximum torque increased with the concentration of Si-69 up to 6 %. The polysiloxane formed during the cure characterization test was responsible for the slightly decreased torque after 6% of Si-69 treatment. Nonetheless, even with high concentration of Si-69 used, torque was still higher than that of untreated PSi filled NR. This is widely understood that sulfur atoms in Si-69 molecule are able to participate in the bonding between rubber and silane molecules resulted in the enhancement of crosslink density of the vulcanizate rubber. The increased of modulus at 200 % elongation, tensile strength under tension, with the silane concentration, was evidence of the crosslink enhancement. Tear strength and hardness of the vulcanizates exhibiting the increment, with the silane used, also clearly confirmed the bonding between Si-69 and rubber molecules. It was elucidated from the research that excess of Si-69 would lead to polysiloxane formation, cluster form of silane and crosslinking density. Scanning Electron Microscope (SEM) micrographs and swelling test are also presented to confirm the phenomena.


1954 ◽  
Vol 27 (1) ◽  
pp. 209-222 ◽  
Author(s):  
W. P. Fletcher ◽  
A. N. Gent

Abstract Measurements are described of the dynamic properties of rubber, loaded with various amounts and types of filler, when subjected to mechanical vibration in simple shear at amplitudes from 0 to 3 per cent shear in the frequency range 20 to 120 c.p.s. The decrease of dynamic modulus with increasing amplitude is shown, for a wide range of filler types and concentrations, to be determined by the amount of stiffening produced by the filler. This relationship is not influenced by variations in the vulcanizing ingredients, reasonable variations in state of vulcanization, addition of softener, or imposition of static shear strain. Rubber compounds stiffened by mixture with, or chemical combination of, other polymers exhibit a smaller order of nonlinearity than that described above and also exhibit much lower hysteresis values within the amplitude range 0 to 3 per cent shear.


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