The Goodyear & Tire Rubber Company

Joginder Lal

Paul Harry Sandstrom

Michael Leslie Senyek

Sandra J Walters

Richard Robinson Smith

Morford C Throckmorton

There is disclosed a rubbery composition comprising a blend of between 95/5 and 5/95 weight percent of (1) a rubbery interpolymer consisting of (a) at least 80 weight percent of at least one .alpha.-olefin containing from 5 to 10 carbon atoms and (b) up to 20 weight percent of a nonconjugated polyene containing from 5 to 30 carbon atoms with (2) a saturated polymer of an .alpha.-olefin oxide prepared from at least one monomer having the structure: ##STR1## wherein R.sub.1 and R.sub.2 are selected from the group consisting of hydrogen or a lower alkyl radical containing from 1 to 8 carbon atoms and R.sub.3 and R.sub.4 are selected from the group consisting of hydrogen, a lower alkyl radical containing from 1 to 8 carbon atoms and an alkoxyalkyl radical containing up to 12 carbon atoms, an aryl radical, a haloalkyl radical containing from 1 to 12 carbon atoms and in which R.sub.3 and R.sub.4 taken together may be trimethylene, tetramethylene, or hexamethylene, thereby forming a cyclic epoxide, or (3) an unsaturated copolymer of an .alpha.-olefin oxide prepared from 80 to 99.5 weight percent of at least one monomer having the structure I; with from 0.5 to 20 weight percent of a comonomer selected from the group consisting of butadiene monoxide, isoprene monoxide, 1,2-epoxy-3-allyloxypropane (allyl glycidyl ether), 4,5-epoxy-1-hexene, 4,5-epoxy-2-hexene, 1,5-cyclooctadiene monoepoxide, 1-vinyl-3,4-epoxycyclohexane and limonene monoxide.

Blends of higher .alpha.- olefin polymers and 1,2-epoxide polymers

Interpolymers of alpha-olefins and nonconjugated alpha,omega-dienes are prepared by organoaluminum compound-transition metal compound catalysts modified with hexaalkylphosphoric triamides or organophosphate esters.

Preparation of interpolymers of alpha-olefins and nonconjugated alpha,

Blends of higher alpha-olefin polymers and 1,2-epoxide polymers

This invention discloses a process for the nonaqueous dispersion polymerization of butadiene monomer in a reaction mixture containing a liquid nonaqueous dispersion medium, the improvement which comprises carrying out the polymerization of the butadiene monomer in the presence of at least one carbonylated polymer.

Process for nonaqueous dispersion polymerization of butadiene in the

The green strength of compositions containing elastomers and/or up to 100 percent of reclaimed rubber is improved by the addition of crystalline or semi-crystalline butene polymers selected from the group consisting of polybutene and interpolymers made from 1-butene with at least one monomer selected from the group consisting of alpha-olefins, non-conjugated dienes, and non-conjugated polyenes. Although reclaimed rubbers are utilized, an unexpected increase in green strength of an unvulcanized blend is obtained. The reclaimed rubbers utilized in the blend may be those which have been devulcanized by mechanical energy, heat, and/or chemical agents. Additionally and preferably, the rubbers may be reclaimed through the use of microwave energy. Additionally, the unvulcanized properties of compositions containing 100 percent of scrap rubber which has been reclaimed using microwave energy are significantly improved by adding crystalline or semi-crystalline alpha-olefin polymers, such as polyethylene or polypropylene. Unexpected improvements in solvent resistance and molding properties of the uncured blends are also achieved.

Composition and method of improving the unvulcanized properties of

New compositions and a process for the preparation of conjugated diene polymers of broadened molecular weight distribution by reacting non-terminated lithium catalyzed conjugated diene polymers with cyclic organic compounds selected from the group of carbonates, thiocarbonates and sulfites. The resulting new compositions are suitable for use in making high impact plastics and for fabricating rubber goods.

Cyclic organo carbonate and sulfite coupling agents for living polymers

New compositions and a process for the preparation of conjugated diene polymers of broadened molecular weight distribution by reacting non-terminated lithium catalyzed conjugated diene polymers with linear organic compounds selected from the group of carbonates, thiocarbonates and sulfites. The resulting new compositions are suitable for use in making high impact plastics and for fabricating rubber goods.

Linear organo carbonate coupling agents for living polymers of

Interpolymers of alpha-olefins and nonconjugated alpha, omega-polyenes are prepared by organoaluminum compound-transition metal compound catalysts modified with hexaalkylphosphoric triamides or at least one compound of the formula Q=P(X Y).sub.3, wherein P is phosphorous, Q is oxygen or sulfur, X is oxygen or sulfur and Y is a hydrocarbon radical containing 1 to 20 carbon atoms.

The invention relates to elastomer composites which can be used for pneumatic tire sidewalls. Such composite particularly comprises a manipulated blend of (A) a hexadiene polymer, (B) high unsaturation rubber, and optionally, (C) a low unsaturation rubber. The sidewall composition particularly enhances the adhesion of the sidewall to the tire carcass stock.

Rubber composites suitable for tire sidewalls from hexadiene polymer

The green strength of elastomers is improved by the addition of semi-crystalline butene polymers selected from the class consisting of polybutene and interpolymers made from 1-butene monomer and at least one monomer selected from the class consisting of alpha-olefins, non-conjugated dienes, and non-conjugated polyenes. The semi-crystalline butene polymer is mixed with a desired elastomer such as natural or synthetic cis-1,4-polyisoprene, or a synthetic elastomer made from monomers selected from the class consisting of conjugated dienes having from 4 to 10 carbon atoms, interpolymers of said dienes among themselves or with vinyl substituted aromatic hydrocarbon compounds having from 8 to 12 carbon atoms, or polyalkenylenes. The mixing or blending of the butene polymer and the elastomer may be through conventional methods such as cement mixing or mastication.

Composition and method of improving the green strength of unvulcanized

There is disclosed a process for selectively cyclizing block polymers which comprises reacting 1 to 30 percent by weight solution of a block copolymer comprised of at least two different blocks, at least one of which blocks is a cyclizable block derived from a conjugated diene monomer of the general structure ##STR1## wherein: R.sub.1 is selected from a hydrocarbyl group containing one to twelve carbon atoms, R.sub.2 is selected from hydrogen or a hydrocarbyl group containing one to twelve carbon atoms; and at least one of which blocks is a non-cyclizable block derived from at least one member selected from the following classes of compounds:

Selective cyclization of block copolymers

The green strength of elastomers is improved by the addition of semi-crystalline butene polymers selected from the class consisting of polybutene and interpolymers made from 1-butene monomer and at least one monomer selected from the class consisting of alpha-olefins, non-conjugated dienes, and non-conjugated polyenes. The blend composition may also include reclaimed rubber. The semi-crystalline butene polymer is mixed with a desired elastomer such as natural or synthetic cis-1,4-polyisoprene, or a synthetic elastomer made from monomers selected from the class consisting of conjugated dienes having from 4 to 10 carbon atoms, interpolymers of said dienes among themselves or with vinyl substituted aromatic hydrocarbon compounds having from 8 to 12 carbon atoms, or polyalkenylenes. The mixing or blending of the butene polymer and the elastomer may be through conventional methods such as cement mixing or mastication.

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Akron, OH, United States of America

Joginder Lal