Effect on Vulcanized Rubber Compounds of Immersion in Boiling Water

1931 ◽  
Vol 23 (6) ◽  
pp. 654-658 ◽  
Author(s):  
K. J. Soule
Keyword(s):  
Boiling Water ◽  
Vulcanized Rubber ◽  
Rubber Compounds

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.

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.

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.

The Effect of Excess Silane-69 Used for Surface Modification on Cure Characteristic and Mechanical Properties of Precipitated Silica Filled Natural Rubber (PSi/NR)

2009 ◽  
Vol 79-82 ◽  
pp. 2171-2174 ◽  
Author(s):  
Chanchai Thongpin ◽  
C. Sangnil ◽  
P. Suerkong ◽  
A. Pongpilaiprertti ◽  
Narongrit Sombatsompop
Keyword(s):  
Mechanical Properties ◽  
Surface Modification ◽  
Crosslinking Density ◽  
High Concentration ◽  
Precipitated Silica ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Cure Time ◽  
Cure Characteristic ◽  
Characterization Test

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.

Nonlinearity in the Dynamic Properties of Vulcanized Rubber Compounds

1954 ◽  
Vol 27 (1) ◽  
pp. 209-222 ◽  
Author(s):  
W. P. Fletcher ◽  
A. N. Gent
Keyword(s):  
Simple Shear ◽  
Dynamic Modulus ◽  
Dynamic Properties ◽  
Mechanical Vibration ◽  
Frequency Range ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Chemical Combination ◽  
Wide Range ◽  
Static Shear

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.

The Impact Resiliometer

1934 ◽  
Vol 7 (3) ◽  
pp. 591-598 ◽  
Author(s):  
Paul Lüpke
Keyword(s):  
Elastic Properties ◽  
Physical Science ◽  
Sustained Load ◽  
Plastic Properties ◽  
Dual Nature ◽  
Hardness Tester ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
The Impact ◽  
Average User

Abstract Original Purpose The writer's first conception of an instrument for quickly measuring the resilience of rubber samples arose in connection with the basic idea for and development of the present A.S.T.M. hardness tester, in an endeavor to provide a reproducible means of measuring and expressing those properties of rubber compounds superficially apparent to the average user. It seemed that if the resistance to pressure (indenting or flexing) and the pressure, or force, of recovery, of a sample were duplicated, the article produced would “feel” the same as the sample, and under normal conditions of use would act mechanically the same. Nature of Problem This problem of measurement, as is generally known, is complicated by the time-hysteresis characteristic of vulcanized rubber compounds, arising through a dual nature, and causing them to manifest both elastic and plastic properties. Any instrument which applies load momentarily measures the almost purely elastic properties, while one which applies a more or less sustained load measures elastic properties modified by the material's partially plastic nature. These ideas are expressed from commercial and industrial viewpoints without regard to their possible deviations from the strict definitions accepted in physical science.

Preliminary Study on Curing of Thick Rubber Article

2015 ◽  
Vol 1134 ◽  
pp. 23-27
Author(s):  
Siti Zulaikha Ibrahim ◽  
Che Mohd Som Said ◽  
Mohamad Asri Ahmad ◽  
Azemi Samsuri
Keyword(s):  
Tensile Strength ◽  
Temperature Region ◽  
The State ◽  
Curing Temperature ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Cure Time ◽  
Zinc Diethyldithiocarbamate ◽  
Preliminary Study ◽  
Rubber Article

In this study, several batches of natural rubber (SMR L) were compounded with three different types of accelerators, which were N-cyclohexylbenzothiazole-2-sulphenamide (CBS), diphenylguanidine (DPG) and zinc diethyldithiocarbamate (ZDEC). ZDEC is known as an ultrafast accelerator. The rubber compounds were cured at 140°C, 130°C, 120°C, 110°C and 100°C in accordance with the temperature gradients observed within the thick rubber block. The main aim of this study is to cure the rubber at each temperature region to the same cure time as that of the outermost region (20 minutes at 140°C). The amount of sulfur and accelerator were adjusted accordingly at each curing temperature to match the state of cure at 140°C. The state of cure of of the vulcanized rubbers were measured using hardness and tensile strength. The same state of cure is achieved if the hardness and tensile strength value are within ±2 IRHD and ±3 MPa, respectively with that of the control vulcanized rubber (hardness and tensile strength cured at 140°C). The results shows that the hardness and tensile strength of the vulcanized rubber at each temperature region are within the expected margins. The results clearly indicated that the type and amount of accelerators, and the amount of sulfur were correctly chosen at each temperature.

PROMOTING INTERFACIAL COMPATIBILITY OF SILICA-REINFORCED NATURAL RUBBER TIRE COMPOUNDS BY ALIPHATIC AMINE

2018 ◽  
Vol 91 (2) ◽  
pp. 433-452 ◽  
Author(s):  
C. Hayichelaeh ◽  
L. A. E. M. Reuvekamp ◽  
W. K. Dierkes ◽  
A. Blume ◽  
J. W. M. Noordermeer ◽  
...  
Keyword(s):  
Crosslink Density ◽  
Silica Surface ◽  
Shielding Effect ◽  
Polymer Layer ◽  
Vulcanized Rubber ◽  
Rubber Compounds ◽  
Bound Rubber ◽  
Interfacial Compatibility ◽  
Physical Interactions ◽  
Tan Δ

ABSTRACT Octadecylamine (OCT) as an alternative for diphenyl guanidine (DPG) in silica-reinforced NR tire compounds with bis-(triethoxysilyl-propyl)tetrasulfide (TESPT) as silane coupling agent was investigated with focus on the improvement of compatibility between the silica surface and rubber molecules, by taking the amine-free rubber compound as a reference. The quantity of OCT and DPG was varied in a range of 2.4–9.5 mmol per 100 parts of rubber by weight (i.e., 0.5–2.5 phr). Bound rubber contents, changes in heat capacity (ΔCp), and immobilized polymer layer (χim) data prove an enhanced interfacial compatibility as the amines are absorbed on the polar silica surface and catalyze the silanization reaction. Comparing the two different amine types, the rubber compounds with OCT show higher interfacial compatibility than the ones with DPG, because of an additional shielding effect promoted by the long alkyl chain that leads to more hydrophobicity. Thus, the rubber compounds with OCT show higher physically bound rubber contents and consequently higher total bound rubber, a higher immobilized polymer layer, as well as a lower Payne effect. However, the compounds with OCT show a higher flocculation rate constant because the physical interactions between amine and silanol groups decrease under thermal treatment. The compounds with OCT show a lower cure torque difference that indicates a lower crosslink density, but because of the good interfacial interaction combining both chemical and physical interactions, the vulcanized rubber with OCT at optimum loading shows better mechanical properties and tan δ at 60 °C when compared with the DPG counterpart. At high (excessive) loading of amines, the compounds with DPG clearly have higher crosslink density and thus higher modulus as well as tensile strength compared with the use of OCT.

Sign in / Sign up

Export Citation Format

Share Document