The Goodyear & Tire Rubber Company

Eilert A Ofstead

Lawson G Wideman

Anthony J Bell

Syed K Mowdood

Walter H Waddell

Jimmy L Richards

Jerry L Brenner

Derek Shuttleworth

Michael Leslie Senyek

Ken W Donbar

Ronald Lee Holsapple

This invention discloses an aqueous slurry for coating the surface of rubber slabs or pellets to reduce the tendency of the rubber slabs or pellets to stick together, said aqueous slurry being comprised of (1) from about 1 weight percent to about 15 weight percent of syndiotactic-1,2-polybutadiene having a melting point of no more than about 140.degree. C. and a particle size of no more than about 40 mesh; (2) from about 0.1 weight percent to about 5 weight percent of a suspending agent; (3) from about 0.05 weight percent to about 2 weight percent of a wetting agent; and (4) from about 78 weight percent to about 98 weight percent water. The present invention further reveals a coated rubber slab having resistance to sticking which is comprised of a rubber slab having a coating thereon, wherein said coating is comprised of syndiotactic-1,2-polybutadiene having a melting point of no more than about 140.degree. C. and a particle size of no more than about 40 mesh.

Partitioning agent for rubber

This invention is directed to treating the surfaces of rubber-reinforcing materials with a gas plasma of O.sub.2 and CF.sub.4 to activate the surfaces to make them more receptive to adhesives. Optionally the surfaces of the reinforcing materials may be exposed to a polymerizing gas plasma such as a thio-carbon to coat the surfaces of the reinforcing material with substances that promote adhesion to rubber. The treated surfaces have been shown to adhere directly to rubber when vulcanized in the normal fashion.

Process for the surface treatment of polymers for

Pure syndiotactic 1,2-polybutadiene is a thermoplastic resin which has double bonds attached in an alternating fashion to its polymeric backbone. Films, fibers and molded articles can be made utilizing syndiotactic 1,2-polybutadiene. It can also be blended into rubbers and cocured therewith. Syndiotactic 1,2-polybutadiene can be made by solution, emulsion or suspension polymerization. It typically has a melting point which is within the range of about 195.degree. C. to about 215.degree. C. However, it is often desirable for the syndiotactic 1,2-polybutadiene to have a melting point of less than about 195.degree. C. This invention discloses a process for preparing syndiotactic 1,2-polybutadiene having a melting point of less than about 195.degree. C. which comprises: polymerizing 1,3-butadiene monomer in an aqueous medium in the presence of (1) a catalyst composition which is made by reacting (a) at least one cobalt compound (b) at least one organoaluminum compound, and (c) at least one conjugated diene; (2) carbon disulfide; and (3) at least one modifier selected from the group consisting of (a) 4-(alkylamino)benzaldehydes, (b) 4-(dialkylamino)benzaldehydes, (c) 2,4-di-(alkoxy)benzaldehydes, (d) 2,6-di-(alkoxy)benzaldehydes, (e) 2,4,6-tri-(alkoxy)benzaldehydes, and (f) 4-(1-azacycloalkyl)benzaldehydes.

Syndiotactic 1,2-polybutadiene synthesis in an aqueous medium

There is disclosed a process for the preparation of gel-free rubbery copolymers of cyclopentene and dicyclopentadiene by means of a catalyst system comprising (A) a soluble tungsten halide or oxyhalide, (B) an organoaluminum compound, (C) an alcohol and (D) a polyhalogenated phenol.

Cyclopentene copolymerization process

There is disclosed a process for the preparation of polymers of cyclopentene or copolymers of cyclopentene with non-conjugated unsaturated alicyclic compounds containing at least 7 carbon atoms in the ring and at least one double bond in the ring or polycyclic olefins or non-conjugated diolefins by the use of the catalyst system comprising (a) tungsten halides or oxyhalides, (b) an organoaluminum compound, (c) an alcohol, and (d) a halogenated phenol.

Process for the preparation of polymers of cyclopentene or copolymers of

There is disclosed a process for the preparation of cyclopentene which comprises selectively hydrogenating cyclopentadiene in the liquid phase by contacting cyclopentadiene with hydrogen in the presence of a hydrogenation catalyst comprising a highly dispersed form of nickel in which a substantial amount of water and certain surfactants are employed in the reaction mixture.

Hydrogenation using surfactants

There is disclosed a cycloolefin metathesis process comprising polymerizing (1) an unsaturated alicyclic compound containing 5 carbons and one double bond in the ring and (2) polycyclic non-conjugated diolefins by the use of a catalyst system comprising (a) tungsten halides and oxyhalides, (b) at least one compound such as alkylaluminum sesquihalides, dialkylaluminum halides, alkylaluminum diahlides or trialkylaluminums, (c) an alcohol, and (d) pentachlorophenol or pentabromophenol.

Process for the polymerization of cycloolefins

There is disclosed a process for the preparation of cyclopentene which comprises selectively hydrogenating cyclopentadiene in the liquid phase by contacting cyclopentadiene with hydrogen in the presence of a hydrogenation catalyst comprising a highly dispersed form of nickel in which water is employed in the reaction medium.

Selective hydrogenation of cyclopentadiene to cyclopentene using Raney

There is disclosed a new process for ring-opening polymerization of cycloolefins by the use of a catalyst comprising (A) tungsten or molybdenum halides, (B) alkyl aluminum halides and (C) alkoxysilanes. Also the catalyst is disclosed as useful in metathesis of olefins.

Metathesis polymerization of cycloolefins

There is disclosed a new process for ring-opening polymerization of cycloolefins by the use of a catalyst comprising (A) tungsten or molybdenum halides, (B) alkyl aluminum halides and (C) an alcohol which has a nitrile substituent. Also the catalyst is disclosed as useful in metathesis of olefins.

Catalyst for metathesis of cycloolefins

There is disclosed a new process for ring-opening polymerization of cycloolefins by the use of a catalyst comprising (A) tungsten or molybdenum halides, (B) alkyl aluminum halides and (C) an alcohol which may optionally contain a halogen substituent and (D) an alcohol which has a nitrile substituent. Also the catalyst is disclosed as useful in metathesis of olefins.

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Cuyahoga Falls, OH, United States of America

Eilert A Ofstead