Asymmetric block copolymers and corresponding adhesive formulations

Claim 2

A block copolymer having the star-shaped, asymmetrical structure (A--B).sub.x Y--C).sub.z where A is a polymer block of a monoalkenyl arene, B is a polymer block of a conjugated diene, C is a polymer block of a conjugated diene, Y is the residue of a multifunctional coupling agent, the sum of x plus z is greater than 6 and less than about 25, the ratio of x to z is between about 5 to 1 and about 1 to 5, the molecular weight of each block A is between about 3,000 and about 30,000, the molecular weight of each block B is between about 15,000 and about 100,000, and the molecular weight of each block C is between about 15,000 and about 100,000.

Claim 3

The block copolymer of claim 1 wherein said A block is a polystyrene block and said B blocks and said C blocks are selected from the group consisting of polybutadiene blocks, polyisoprene blocks and poly(butadiene-isoprene)blocks.

Claim 4

The block copolymer of claim 2 wherein said B blocks and said C blocks are polyisoprene blocks.

Claim 5

The block copolymer of claim 1 wherein x is an integer between 2 and 28 and z is an integer between 2 and 28.

Claim 6

The block copolymer of claim 1 wherein Y is the residue of a polyalkenyl aromatic coupling agent.

Claim 7

The block copolymer of claim 5 wherein said coupling agent is divinyl benzene.

Claim 8

The process for preparing the block copolymer of claim 1 comprising: (a) solution polymerizing a monalkenyl arene under polymerization conditions at a temperature between about -75° C. to +150° C. with an organomonolithium compound, therein forming a living A-Li polymer arm having a molecular weight between about 3,000 and 30,000; (b) contacting said living A-Li polymer arm with a conjugated diene monomer therein forming a living AB-Li polymer arm having a molecular weight between about 15,000 and 100,000; (c) solution polymerizing a conjugated diene under polymerization conditions at a temperature between about -75° C. to +150° C. with an organomonolithium compound, therein forming a living C-Li polymer arm having a molecular weight between about 15,000 and 100,000; (d) mixing the solution of living AB-Li polymer arms with the solution of living C-Li polymer arms; and (e) contacting the resulting mixture with at least 0.5 mole per mole of living polymer of a multifunctional coupling agent at a temperature between about 0° C. and about 150° C. therein forming said, asymmetric star-shaped polymer.

Claim 9

The process according to claim 7 wherein said multifunctional coupling agent is a polyalkenyl aromatic coupling agent.

Claim 10

The process according to claim 8 wherein said polyalkenyl aromatic coupling agent is divinyl benzene.

Claim 11

The process for preparing the block copolymer of claim 1 wherein the conjugated diene employed for block B is the same as the conjugated diene employed for block C, said process comprising: (a) solution polymerizing a monoalkenyl arene under polymerization conditions at a temperature between about -75° C. to +150° C. with an organomonolithium compound, therein forming a living A-Li polymer arm having a molecular weight between about 3,000 and 30,000; (b) adding an additional amount of organomonolithium compound to the solution of living A-Li polymer arms; (c) contacting the resulting solution with a conjugated diene monomer therein forming a mixture of living AB-Li arms and living C-Li arms each having a molecular weight between about 15,000 and 100,000; and (d) contacting the resulting mixture with at least 0.5 mole per mole of living polymer of a multifunctional coupling agent at a temperature between about 0° C. and about 150° C., therein forming said, asymmetric star-shaped polymer.

Claim 12

The process according to claim 10 wherein said multifunctional coupling agent is a polyalkenyl aromatic coupling agent.

Claim 13

The process according to claim 11 wherein said polyalkenyl aromatic coupling agent is divinyl benzene.

Claim 14

A selectively hydrogenated block copolymer having the star-shaped, asymmetrical structure (A--B).sub.x Y--C).sub.z where A is a polymer block of a monoalkenyl arene, B is a substantially hydrogenated polymer block of a conjugated diene, C is a substantially hydrogenated polymer block of a conjugated diene, Y is the residue of a multifunctional coupling agent, the sum of x plus z is greater than 6 and less than about 25, the ratio of x to z is between about 5 to 1 and about 1 to 5 and the molecular weight of each block A is between about 3,000 and about 30,000, the molecular weight of each block B is between about 15,000 and about 100,000, and the molecular weight of each block C is between about 15,000 and about 100,000.

Claim 15

A selectively hydrogenated block copolymer having the star-shaped, asymmetrical structure (A--B).sub.x Y--C).sub.z where A is a polymer block of a monoalkenyl arene, B is a substantially hydrogenated polymer block of a conjugated diene, C is a substantially hydrogenated polymer block of a conjugated diene, Y is the residue of a multifunctional coupling agent, the sum of x plus z is greater than 6 and less than about 25, the ratio of x to z is between about 5 to 1 and about 1 to 5 and the molecular weight of each block A is between about 3,000 and about 30,000, the molecular weight of each block B is between about 15,000 and about 100,000, and the molecular weight of each block C is between about 15,000 and about 100,000.

Claim 16

The block copolymer of claim 13 wherein said A block is a polystyrene block and said B blocks and said C blocks are selected from the group consisting of substantially hydrogenated polybutadiene blocks, substantially hydrogenated polyisoprene blocks and substantially hydrogenated poly(butadiene-isoprene) blocks.

Claim 17

The block copolymer of claim 13 wherein x is an integer between 2 and 28 and z is an integer between 2 and 28.

Claim 18

The block copolymer of claim 13 wherein Y is the residue of a polyalkenyl aromatic coupling agent.

Claim 19

The block copolymer of claim 16 wherein said coupling agent is divinyl benzene.