Block copolymers of Ziegler-Natta polymerized and anionically polymerized monomers

Claim 2

A process for preparing living multi-block copolymers comprising; (a) combining under polymerization conditions one or more alpha olefin monomers in a suitable diluent in the presence of a Ziegler-Natta catalyst system and a transmetallation reagent selected from the group consisting of dialkyl zinc, dialkyl cadmium, tetralkyl lead, and their salts, (b) contacting the resulting polymer with an anionic transfer reagent generating an anionic polymerization initiator thereby forming living polymer chains, (c) contacting the resulting living polymer chains sequentially with one or more monomers selected from the group consisting of conjugated dienes, and monoalkenylarenes and activated mono olefins; (d) recovering multi-block copolymers.

Claim 3

A process for preparing block copolymers comprising: (a) combining under polymerization conditions one or more alpha-olefin, monomers, a Ziegler-Natta catalyst, a transmetallation reagent in a suitable diluent; (b) contacting the resulting polymer with an anionic polymerization transfer reagent selected from the group consisting of MeOLi, EtOLi, PrOLi, BuOLi, hexyl and octyl alkoxides of lithium, thereby forming living polymer chains; (c) contacting the resulting living polymer chains sequentially with one or more monomers selected from the groups consisting conjugated dienes monoalkenylarenes and activated monoolefins thereby forming living multi block copolymers; (d) contacting the resulting living multi block copolymers with a coupling agent having a functionality of two or more; and (e) recovering the resulting block copolymer.

Claim 4

A process for preparing block copolymers comprising: (a) combining under polymerization conditions one or more alpha-olefin, monomers, a Ziegler-Natta catalyst, a transmetallation reagent in a suitable diluent; (b) contacting the resulting polymer with an anionic polymerization transfer reagent selected from the group consisting of MeOLi, EtOLi, PrOLi, BuOLi, hexyl and octyl alkoxides of lithium, thereby forming living polymer chains; (c) contacting the resulting living polymer chains sequentially with one or more monomers selected from the groups consisting conjugated dienes monoalkenylarenes and activated monoolefins thereby forming living multi block copolymers; (d) contacting the resulting living multi block copolymers with a coupling agent having a functionality of two or more; and (e) recovering the resulting block copolymer.

Claim 5

The process according to claim 1 wherein said alpha-olefin monomer is ethylene, propylene, 1-butene or a mixture.

Claim 6

The process according to claim 1 wherein said hydrocarbon diluent is n-hexane, n-heptane, cyclohexane, cyclopentane, benzene, toluene, one or more xylenes, 2,2,4-trimethylpentane, or mixture, or monomers themselves.

Claim 7

The process of claim 1 wherein the Ziegler-Natta catalyst is an organo-aluminum/TiCl 3 catlayst.

Claim 8

The process of claim 1 wherein the Ziegler-Natta catalyst is triethylaluminum/TiCl 3 .

Claim 9

The process of claim 1 wherein the Ziegler-Natta catalyst is diethylaluminum chloride/TiCl 3 .

Claim 10

The process of claim 1 wherein the Ziegler-Natta catalyst is present at between 0.3 and 30 millimoles per hundred grams of monomer.

Claim 11

The process of claim 1 wherein the transmetallation reagent is diethyl zinc.

Claim 12

The process of claim 1 wherein the Ziegler-Natta polymerization takes place at a temperature between about 30° C. and about 80° C., a pressure sufficient to maintain the mixture substantially liquid and continues for between 15 minutes and 8 hours.

Claim 13

The process according to claim 1 wherein said transfer agent is n-butyllithium, sec-butyllithium, n-decyllithium, phenyllithium, 1-naphthyllithium, p-tolyllithium, cyclohexllithium, eicosyllithium or their alkoxides or mixture.

Claim 14

The process according to claim 1 wherein said conjugated diene is 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 2-methyl-1,3-pentadiene, 2,3-dimethyl-1,3-pentadiene, 2-methyl-3-ethyl-1,3-pentadiene, 2-methyl-1,3-butadiene or mixture.

Claim 15

The process of claim 1 wherein the monoalkylarene is styrene or alkylstyrene.

Claim 16

The process of claim 1 wherein the anionic polymerization takes place at between 20° C. and 120° C. for between 2 minutes and 8 hours.

Claim 17

The process according to claim 1 wherein said polymerization admixture, after polymerization of said conjugated diene monomer is treated with a lower alcohol, acid, or water.

Claim 18

The process according to claim 2 wherein said alpha-olefin monomer is ethylene, propylene, 1-butene or a mixture.

Claim 19

The process according to claim 2 wherein said hydrocarbon diluent is n-hexane, n-heptane, cyclohexane, cyclopentane, benzene, toluene, one or more xylenes, 2,2,4-trimethylpentane, or mixture or monomer.

Claim 20

The process of claim 2 wherein the Ziegler-Natta catalyst is an organo-aluminum/TiCl 3 catlayst.

Claim 21

The process of claim 2 wherein the Ziegler-Natta catalyst is triethylaluminum/TiCl 3 .

Claim 22

The process according to claim 2 wherein said hydrocarbon diluent is Et 2 AlCl/TiCl 3 .

Claim 23

The process of claim 2 wherein the Ziegler-Natta catalyst is present at between 0.3 and 30 millimoles per hundred grams of monomer.

Claim 24

The process of claim 2 wherein the transmetallation reagent is diethyl zinc.

Claim 25

The process of claim 2 wherein the Ziegler-Natta polymerization takes place at a temperature between about 30° C. and about 80° C., a pressure sufficient to maintain the mixture substantially slurry and continues for between 15 minutes and 8 hours.

Claim 26

The process according to claim 2 wherein said initiator is n-butyllithium, sec-butyllithium, n-decyllithium, phenyllithium, 1-naphthyllithium, p-tolyllithium, cyclohexllithium, eicosyllithium or their alkoxides or mixture.

Claim 27

The process according to claim 2 wherein said conjugated diene is 1,3-butadiene, isopresne, 2,3-dimethyl-1,3-butadiene, 2-methyl-1,3-pentadiene, 2,3-dimethyl-1,3-pentadiene, 2-methyl-3-ethyl-1,3-pentadiene, 2-methyl-1,3-butadiene or mixture.

Claim 28

The process of claim 2 wherein the monoalkylarene is styrene or alklystyrene.

Claim 29

The process of claim 2 wherein the anionic polymerization takes place at between 30° C. and 120° C. for between 2 minutes and 8 hours.

Claim 30

The process according to claim 2 wherein said coupling agent is present in the range of about 0.5 to 10 equivalents per equivalent of lithium, thereby preparing a coupled polymer.

Claim 31

The process according to claim 2 wherein said coupling agent is a polyepoxide, polyisocyanate, polyamine, polyaldehyde, polyketone, polyanhydride, polyester, polyhalide, polyvinyl aromatic, carbon dioxide, or monoester, wherein the functionality of said agent is at least 2.

Claim 32

The process according to claim 2 employing 1-butene as said alpha-olefin monomer, heptane as said diluent, n-butyllithium as said hydrocarbon monolithium initiator, 1,3-butadiene as said conjugated diene; and wherein coupling is by treatment with silicon tetrahalide.

Claim 33

The process according to claim 2 employing silicon tetrachloride as said silicon tetrahalide.

Claim 34

The block copolymer product produced by the process of claim 1.

Claim 35

The block copolymer product produced by the process of claim 2.

Claim 36

The end-capped block copolymer product produced by the process of claim 1.