Styrene-Diene Resins in Rubber Compounding

1947 ◽  
Vol 20 (1) ◽  
pp. 241-248
Author(s):  
A. M. Borders ◽  
R. D. Juve ◽  
L. D. Hess

Abstract Early in the investigation of butadiene-styrene copolymers as synthetic rubbers, this laboratory became interested in copolymers containing much more styrene than any of the American or German synthetics. This interest was soon directed to the resinous copolymers obtained when the styrene content is increased beyond the range in which rubberlike properties are observed at room temperature. The exploratory work, therefore, involved preparation and evaluation of butadiene-styrene copolymers containing from 65 to 98 per cent styrene. No description of similar polymers has been found. Konrad and Ludwig claimed the improvement of rubberlike properties of butadiene-styrene copolymers by increasing the styrene content from the normal range to “between about 47.5 and about 70 per cent”. The claims and examples of this patent emphasize the improvement of rubberlike properties, such as tensile, elongation, and rebound, at high temperatures. It is well known in this country, however, that increase in styrene content beyond a certain point, perhaps 50–55 per cent, is accompanied by a loss of overall balance of rubber characteristics. Therefore, the copolymers at the upper end of the range described by Konrad and Ludwig have definite limitations for rubber uses—for example, low rebound, high brittle point, shortness, etc. In the writers' laboratory useful resins have been prepared from dienes and vinyl aryl hydrocarbons in the range 5 to 20 per cent diene and 80 to 95 per cent vinyl aryl hydrocarbon. This paper describes the properties and certain uses of one of these copolymers containing approximately 15 parts of butadiene and 85 parts of styrene. This material possesses a combination of physical and chemical properties which permit its use in several applications where cyclized natural or synthetic rubbers are commonly employed. Cyclized natural rubber has been described by Bruson, Endres, and Thies and Clifford. Cyclized synthetic rubbers were described recently by Endres. One product of this type is made from a special synthetic rubber. The new 15 butadiene—85 styrene copolymer is now identified as Pliolite S-3, since it may be used in many Pliolite applications, often with distinct advantages over either the natural or synthetic rubber derivatives.

Author(s):  
María Leonor Méndez-Hernández ◽  
José Luis Rivera-Armenta ◽  
Zahida Sandoval-Arellano ◽  
Beatriz Adriana Salazar-Cruz ◽  
María Yolanda Chavez-Cinco

2019 ◽  
Vol 35 (3) ◽  
pp. 997-1003
Author(s):  
Sonu Sharma ◽  
Sitansh Sharma ◽  
Niraj Upadhyay

Bitumen is used worldwide in the construction of flexible pavements and because of its wide applicability its performance is needed to be improved in all regards like, Chemical, and thermal stability, fatigue life, moisture susceptibility, mechanical strength, temperature susceptibility, rutting resistance, ageing resistance, tensile strength, viscosity, stiffness etc. In this connection, researchers have used various modifiers to improve the pavement performance. The present paper provides a brief review of different modifiers in road making industry. Some popular polymer modifiers like low density polythene, high density polythene, polypropylene, ethyl vinyl acetate, styrene butadiene styrene and industrial waste are reviewed in terms of their role in bitumen modification. It also discusses enhancement in properties of bitumen after modification in order to improve properties of pavement. Through the reviewed literature, it is found that the addition of the polymers to bitumen tends to enhance fatigue and cracking resistance mainly. The future development and recommendation in modifiers for bitumen modification are also suggested in the end.


1949 ◽  
Vol 22 (4) ◽  
pp. 1084-1091
Author(s):  
D. G. Fisher ◽  
L. Mullins ◽  
J. R. Scott

Abstract Experiments were carried out to explore the possibility of making good electrical ebonites from various types of synthetic rubber. The ebonites produced were tested for permittivity and power factor over wide ranges of temperature and frequency. Thioplasts (Thiokols AZ and FA) apparently do not produce hard ebonitelike vulcanizates by the normal procedure. Neoprenes (GN and I) give ebonites, but with such high dielectric power loss as to be unsuitable for use as high-frequency dielectrics; moreover, if the mix contains zinc oxide, the ebonite has a very hygroscopic and therefore electrically unsatisfactory surface. Butadiene copolymers containing polar groups (butadiene-acrylonitrile types and Thiokol RD) give ebonites with high power loss, hence are not suitable for making high-grade electrical ebonites. Polybutadiene (Buna-85) and butadiene-styrene copolymers (GR-S, Hycar-EP, Buna-S) are much nearer to natural rubber as far as the radio-frequency (100 to 2,500 kc. per sec.) power loss of their ebonites is concerned. The GR-S ebonite examined was not so good as natural rubber at room temperature, but was superior above about 50° C. Buna-85 and Hycar-EP were superior to natural rubber over the whole temperature range; indeed, the high-styrene copolymers, as represented by Hycar-EP and Buna-SS, appear to be the best type of synthetic rubber for making ebonite with low power loss, especially at high frequencies and temperatures. The effects of changing temperature and frequency on permittivity and power factor are discussed. Attention is drawn to the big effect of temperature on power factor; this was less with polybutadiene and butadiene-styrene ebonites than with natural rubber ebonite, in keeping with the greater heat resistance of the former as judged by plastic yield tests. Comparison of the effects of rising temperature and decreasing frequency shows that these produce broadly similar effects on power factor, as would be expected on theoretical grounds, but that rising temperature superposes a second effect (an increase), presumably due to increased ionic conduction.


2007 ◽  
Vol 361-363 ◽  
pp. 463-466
Author(s):  
T. Lin ◽  
S.M. Zhang ◽  
J. Li ◽  
L. Zhang ◽  
Y.H. Liu ◽  
...  

The composite scaffolds with nine different ratios of nano-HA and ß-TCP content were fabricated by using lyophilization method. Their microscopy, physical and chemical properties were investigated by using scanning electron microscopy (SEM), X-ray diffraction (XRD), and fourier transformed infrared (FTIR) spectroscopy. MTT test was applied to quantitatively assess the number of viable cells attached and grown on the scaffolds. And the result showed that the amount of cells on the scaffold containing 30% by mass of nano-HA was significantly higher than the other samples.


1950 ◽  
Vol 23 (4) ◽  
pp. 760-769
Author(s):  
R. D. Juve ◽  
J. W. Marsh

Abstract Synthetic rubbers and natural rubber increase in stiffness at low temperatures and tend to lose their elastic characteristics. This stiffening and hardening phenomenon occurs in varying degrees with various elastomers. Natural rubber and certain synthetic rubbers crystallize during extended exposure at low temperature, whereas other synthetic rubbers such as GR-S remain amorphous. In a general review of the low temperature properties of synthetic rubber, Liska has shown that decreased styrene in butadiene-styrene copolymers improves the flexibility at low temperature. The low temperature flexibility of vulcanized articles made from any particular rubber or synthetic rubber is influenced by the compounding ingredients admixed with the elastomer. This paper shows the results of some studies of the effect of these compounding ingredients on the low temperature serviceability of butadiene-styrene copolymers. Somewhat similar work on the effect of a large number of plasticizers in GR-S has been conducted at the Rubber Laboratory, Mare Island Naval Shipyard, with particular emphasis on compression set at low temperature.


1955 ◽  
Vol 28 (1) ◽  
pp. 51-56
Author(s):  
Lawrence A. Wood

Abstract From Figure 3 one draws the following significant conclusions: (1) Crystallization is not observed if the polymerization temperature is above 60° C. (2) For polymerization at 50° C, a small amount (2 to 6 per cent) of bound styrene inhibits crystallization completely. (3) For polymerizations at 5° C, the limit is at about 15 to 18 per cent bound styrene content. (4) At the lowest polymerization temperatures normally utilized, this limit is at about 30 per cent bound styrene. Direct experimental observation is in general accord with these conclusions.


1949 ◽  
Vol 27f (2) ◽  
pp. 35-46 ◽  
Author(s):  
J. M. Mitchell ◽  
H. Leverne Williams

The copolymerization of styrene and butadiene in ratios in which the styrene equals or predominates over the butadiene on a mass basis is essentially similar to copolymerization in the presence of a predominance of butadiene. However, the rate of reaction and the length of the induction period is increased. Increasing the amount of the dodecyl mercaptan regulator results in a slight increase in rate and diminution of the induction period. The dodecyl mercaptan reacts at a lower rate than during the production of GR–S. The regulating index as defined by the ratio of the logarithm of the residual mercaptan over the conversion is 1.53. The bound styrene and increment styrene curves seem to be normal and indicate reactivity ratios r1 (butadiene) equal to 1.4 to 2.2, r2 equal to 0.5 to 0.7. If these reactivity ratios are corrected for the bifunctional nature of butadiene then the constants for butadiene monomer are Q equal to 0.9 and e equal to − 1. Likewise the gel–viscosity data are similar to those observed with GR–S except that the pre-gel rise in viscosity, the formation of gel, and the slope of the viscosity conversion curves diminish with increasing styrene in the charge. The chain transfer action of styrene is increasingly evident with increasing styrene content in the charge but in all cases the regulating effect of dodecyl mercaptan is still apparent.


1946 ◽  
Vol 19 (4) ◽  
pp. 1077-1084 ◽  
Author(s):  
E. J. Meehan

Abstract The ultraviolet absorption of polystyrene, with maximum absorption at 262 mµ, is due to the presence of phenyl residues in the polymer. The specific extinction coefficient is constant, i.e., independent of the molecular weight of the polymer. This shows that the extinction of the phenyl residues is additive. On the basis of this fact, it is shown that the styrene content of a butadiene-styrene copolymer (such as GR-S rubber) can be determined by ultraviolet spectrophotometry. The relative precision of the determination is about 1 per cent, the probable relative accuracy is about 3 per cent.


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