Low Temperature Behavior of Butadiene-Styrene Copolymers

1949 ◽  
Vol 41 (11) ◽  
pp. 2535-2538
Author(s):  
R. D. Juve ◽  
J. W. Marsh
1948 ◽  
Vol 3 (4) ◽  
pp. 465-480 ◽  
Author(s):  
Karl E. Beu ◽  
W. B. Reynolds ◽  
C. F. Fryling ◽  
H. L. McMurry

1955 ◽  
Vol 28 (2) ◽  
pp. 557-569 ◽  
Author(s):  
D. A. Henderson ◽  
L. A. McLeod

Abstract The second-order transition temperatures of plasticized butadiene-styrene copolymers have been measured by dilatometric techniques. In a series of ester plasticizers, the ability of a given plasticizer to depress the second-order transition temperature of the polymer is related to the swelling effect of the plasticizer on the polymer. The special case of a crystallizing plasticizer (dibutyl sebacate) has been discussed. Common petroleum plasticizers do not appear to behave in a similar manner. The change of coefficient of expansion of the ester-plasticized copolymers is related to the measured transition temperature of the blend.


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.


1948 ◽  
Vol 21 (2) ◽  
pp. 452-460
Author(s):  
A. E. Juve ◽  
M. M. Goff ◽  
C. H. Schroeder ◽  
A. W. Meyer ◽  
M. C. Brooks

Abstract Sodium-catalyzed butadiene-styrene copolymers (S-BS), of composition 75 weight-per cent butadiene: 25 weight-per cent styrene, have been compounded in tread type recipes. Evaluation tests showed properties significantly different from those of GR-S, the emulsion-phase free radical—catalyzed copolymers of identical monomer composition. 1. The processing characteristics of S-BS are considerably superior to those of GR-S, although one experience with a high temperature internal mix may indicate some limitation. Objective laboratory processing tests show that S-BS resembles high-styrene emulsion copolymers in that it can be satisfactorily fabricated from stocks containing less filler than is required in GR-S stocks for similar uses. 2. Stress-strain properties based on limited compounding studies are similar to those of GR-S. 3. The flex crack growth—hysteresis balance for S-BS vulcanizates is much superior to that of GR-S vulcanizates. Vulcanizates of emulsion polymers of high styrene content also had a flex crack growth—hysteresis balance superior to that of GR-S vulcanizates. 4. The low temperature properties of S-BS vulcanizates are inferior to those of GR-S vulcanizates. Brittle points and low temperature Young's modulus of S-BS vulcanizates are much higher than those of GR-S vulcanizates.


1949 ◽  
Vol 22 (2) ◽  
pp. 356-369 ◽  
Author(s):  
Karl E. Beu ◽  
W. B. Reynolds ◽  
C. F. Fryling ◽  
H. L. McMurry

Abstract Although it is now generally recognized that the temperature of polymerization affects profoundly the properties of emulsion elastomers, there is very little evidence available pertaining to the cause of the variations of properties. It is felt by some that the improved properties of low-temperature elastomers can be related to variations in molecular weight and molecular-weight distribution. In this laboratory, however, the opinion has prevailed that the lower emulsion polymerization temperatures appreciably alter the fine structure of the molecules with an increase in the regularity of the polymer chains. If there were actually less branching and cross-linking in low-temperature polymers, and less 1,2-addition to monomer components, the increased order should be evident from x-ray diffraction patterns. To provide information on the above questions, x-ray studies were made with four purposes in view: (1) to determine the effect of polymerization temperature on the crystallization properties of unstretched and stretched polybutadienes; (2) to determine the influence of styrene content on the crystallization of butadiene-styrene copolymers; (3) to study some effects of compounding and vulcanization on crystallizable polybutadiene; and (4) to use the preferred orientation patterns obtained from some of these polymers for structural evaluations. To accomplish these objectives, x-ray patterns were obtained at several temperatures of some unstretched and stretched polybutadiene polymers, butadiene-styrene copolymers, and a vulcanized and compounded polybutadiene. The polybutadienes were prepared by emulsion polymerizations at 55°, 40°, 30°, 20°, 5°, −10° and −20° C. Since the −20° C polybutadiene showed the most marked crystallization patterns, the effects of compounding and of styrene addition were studied, using polymers prepared at this temperature for comparison. Three butadiene-styrene copolymers containing, respectively, 10, 20, and 30 per cent styrene in the monomer charge and one vulcanized polybutadiene compounded with Wyex carbon black were studied.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2249
Author(s):  
Bei Chen ◽  
Fuqiang Dong ◽  
Xin Yu ◽  
Changjiang Zheng

In order to solve the problems caused by asphalt diseases and prolong the life cycle of asphalt pavement, many studies on the properties of modified asphalt have been conducted, especially polyurethane (PU) modified asphalt. This study is to replace part of the styrene-butadiene-styrene (SBS) modifier with waste polyurethane (WP), for preparing WP/SBS composite modified asphalt, as well as exploring its properties and microstructure. On this basis, this paper studied the basic performance of WP/SBS composite modified asphalt with a conventional performance test, to analyze the high- and low-temperature rheological properties, permanent deformation resistance and storage stability of WP/SBS composite modified asphalt by dynamic shear rheometer (DSR) and bending beam rheometer (BBR) tests. The microstructure of WP/SBS composite modified asphalt was also observed by fluorescence microscope (FM) and Fourier transform infrared spectroscopy (FTIR), as well as the reaction between WP and asphalt. According to the results of this study, WP can replace SBS as a modifier to prepare WP/SBS composite modified asphalt with good low-temperature resistance, whose high-temperature performance will be lower than that of SBS modified asphalt. After comprehensive consideration, 4% SBS content and 15% WPU content (4 S/15 W) are determined as the suitable types of WPU/SBS composite modified asphalt.


1974 ◽  
Vol 18 (2) ◽  
pp. 401-418 ◽  
Author(s):  
Norman E. Rustad ◽  
Robert G. Krawiec

2004 ◽  
Vol 279 (1) ◽  
pp. 5-13 ◽  
Author(s):  
M El Massalami ◽  
H.A Borges ◽  
H Takeya ◽  
R.E Rapp ◽  
F.A.B Chaves

1998 ◽  
Vol 177-181 ◽  
pp. 451-452 ◽  
Author(s):  
T. Nishioka ◽  
K. Mizutani ◽  
S. Taniguchi ◽  
M. Kontani

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