Graft copolymerization process

• US 4,107,238 A
• Filed: 01/22/1976
• Issued: 08/15/1978
• Est. Priority Date: 01/22/1976
• Status: Expired due to Term

• Current Assignee: Exxon Research and Engineering Company (Exxon Mobil Corporation)
• Original Assignee: Exxon Research and Engineering Company (Exxon Mobil Corporation)
• Inventors: Langer, Arthur W. Jr., Roper, Robert
• Primary Examiner(s): Michl, Paul R.
• Application Number:
  US05/651,573
• Time in Patent Office: 936 Days
• Field of Search: 260/879, 260/880 R
• US Class Current: 525/250
• CPC Class Codes: C08F 212/08 Styrene
• CPC Class Codes: C08F 255/10 on to butene polymers
• CPC Class Codes: C08F 279/02 on to polymers of conjugated dienes

Abstract

Novel graft copolymers of isobutylene-conjugated diene copolymeric backbones are prepared employing polymer lithiation wherein the polymeric lithiated complex is treated with an ether compound prior to a graft copolymerization reaction with styrene monomer whereby improved grafting efficiencies are obtained.

Claims

1. A method for grafting styrene monomer in high grafting efficiency onto an elastomeric isobutylene-conjugated diene copolymer which comprises the steps of:

(a) forming a solution of the elastomer in an inert hydrocarbon solvent;

(b) treating said solution with an organolithium chelating polyamine composition whereby a polymer lithium polyamine complex is formed;

(c) treating said complex with from 2 to 50 volume % of an organic monoether or polyfunctional ether whereby unreacted organolithium polyamine is decomposed; and

(d) contacting the styrene monomer with the treated complex of step (c) whereby a graft copolymer is formed, at least a major proportion of the reacted styrene monomer being present in said graft copolymer, and said copolymer is a thermoelastomer.

2. The method of claim 1 wherein the elastomer has a conjugated diene content between about 5 and 50 mole %.

3. The method of claim 1 wherein the conjugated diene has 5 to 9 carbon atoms.

4. The method of claim 1 wherein the conjugated diene is isoprene, butadiene, methyl cyclopentadiene, cyclopentadiene, 2,3-dimethylbutadiene or piperylene.

5. The method of claim 1 wherein the ether is tetrahydrofuran.

6. The method of claim 1 wherein the ether treatment step is carried out at a temperature between 20°

and 50°

C.

7. The method of claim 1 wherein the organolithium is n-butyllithium or sec-butyllithium.

8. The method of claim 7 wherein the polyamine is tetramethyl-1,2-ethanediamine.

9. The method of claim 1 wherein the grafting efficiency is at least 70%.

10. A novel thermoelastomeric graft copolymer composition, said copolymer composition consisting essentially of an isobutylene-conjugated diene hydrocarbon copolymer backbone, said diene having 4 to 14 carbon atoms, the diene content being between about 5 and 50 mole percent and grafted copolymerized styrene, the styrene content of said thermoelastomeric graft copolymer being about 20 to 40 weight percent, said graft copolymer composition being prepared according to the process of claim 1.

11. A novel thermoelastomeric graft copolymer composition, said copolymer composition consisting essentially of an isobutylene-conjugated diene hydrocarbon copolymer backbone, said diene having 4 to 14 carbon atoms, the diene content being between about 5 to 50 mole percent and grafted copolymerized styrene, the styrene content of said thermoelastomeric graft copolymer being about 40 to 70 weight percent, said graft copolymer composition being prepared according to the process of claim 1.

12. The composition of claim 10 wherein the diene has 5 to 9 carbon atoms.

13. The composition of claim 11 wherein the diene has 5 to 9 carbon atoms.

14. The composition of claim 10 wherein the diene is isoprene, butadiene, cyclopentadiene, methyl cyclopentadiene, 2,3-dimethylbutadiene or piperylene.

15. The composition of claim 11 wherein the diene is isoprene, butadiene, cyclopentadiene, methyl cyclopentadiene, 2,3-dimethylbutadiene or piperylene.

16. The composition of claim 10 wherein the diene is cyclopentadiene.

17. The composition of claim 10 wherein the diene is isoprene.

18. The composition of claim 10 wherein the diene content is 8 to 35 mole percent.

19. The composition of claim 11 wherein the diene content is 8 to 35 mole percent.