Elastomer Blends

1974 ◽  
Vol 47 (3) ◽  
pp. 481-510 ◽  
Author(s):  
P. J. Corish ◽  
B. D. W. Powell

Abstract Mixtures are difficult to define within the range of materials employed in the rubber and plastic industries. A composite article such as a tire is a mixture of wire (metal), textile cord (organic fiber), and rubber compounds. The rubber compound itself is a mixture of elastomer, filler, and, usually, extender. Moreover, the elastomer may be a mixture of two or more rubbers. On a smaller scale, the elastomer may contain ‘blocky’ segments or crystalline portions along the polymer chains which act as ‘reinforcing’ agents or stiffeners. These may be similar to the repeat units of the elastomeric part, e.g., isotactic—atactic block copolymers of poly(propylene) or poly(propylene oxide); or different from it, as in the stereo block styrene—butadiene thermoplastic copolymers. Two types of elastomer may of course, be copolymerized or one elastomeric type may be grafted onto another. Furthermore, certain catalysts could cause simultaneous homopolymerization of two monomers. All the foregoing systems are different facets of the broad concept of blends, but some selection is obviously needed. In this review, most emphasis will be placed on elastomer—elastomer blends including their preparation from the constituent elastomers. Reference will be made to elastomer—plastic blends prepared from separate materials and by block/graft type reactions. Blends of one plastic with another lie outside the scope of this review.

2019 ◽  
Vol 10 (13) ◽  
pp. 1569-1574 ◽  
Author(s):  
Jan Blankenburg ◽  
Martin Stark ◽  
Holger Frey

Oxidation of tertiary amines leads to multiple amine N-oxide moieties and a highly polar polyether structure. Combination with the apolar poly(propylene oxide) affords unusual surfactants.


1967 ◽  
Vol 40 (4) ◽  
pp. 1183-1199 ◽  
Author(s):  
C. W. Childers ◽  
G. Kraus

Abstract In butadiene styrene copolymers containing long block sequences chain segments associate with like segments to form a two phase structure. Properties of such polymers are dependent not only on composition and molecular weight but also on block sequence along the chain. Polymers containing two or more polystyrene blocks per molecule form networks and exhibit elastomeric properties in the uncured state resembling those of filler reinforced vulcanizates. This behavior is shown both by linear styrene-butadiene-styrene elastomers and multichain block copolymers branched in the polybutadiene blocks. A prominent loss tangent peak was observed around —40° C for the multichain polymers. Stress strain following prestretching and stress relaxation measurements indicate some shifting of polystyrene associations during stretching. Tensile strength is reduced by increasing temperature and addition of plasticizers. Reinforcement by polystyrene domains in vulcanized block copolymers is evident from tensile strength, dynamic modulus, and swelling measurements, but decreases with increased crosslinking. The number of styrene sequences in the primary molecules is less important after vulcanization as crosslinking destroys the individuality of the original polymer chains.


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