IP Library Granted Patent US 11,597,790
Granted Patent B2
US 11,597,790 · App. 17/123,391 · Granted Mar 7, 2023

Synthesis of isoprene-butadiene copolymer rubbers

Inventor: Thomas Franklin Spilker (Broadview Heights, OH)
Assignee: THE GOODYEAR TIRE & RUBBER COMPANY
C08F236/08C08F236/06C08F4/52C08F4/545C08F2800/20
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Quick Facts
Patent No.
US 11,597,790
App. No.
17/123,391
Granted
Mar 7, 2023
Kind
B2
Abstract

It has been unexpectedly found that certain neodymium catalyst systems can be used to copolymerize isoprene and 1,3-butadiene to produce random isoprene-butadiene copolymer rubbers which are not tapered. These random isoprene-butadiene copolymer rubbers have properties which are beneficial for use in rubber formulations for manufacturing a wide variety of rubber products, such as tires, hoses, conveyor belts, power transmission belts, and shoe soles. These random isoprene-butadiene rubbers are synthesized by copolymerizing (a) isoprene monomer or a substituted isoprene monomer and (b) 1,3-butadiene monomer in the presence of a neodymium catalyst system, wherein the neodymium catalyst system is prepared by (1) reacting a neodymium carboxylate with an organoaluminum compound in the presence of a conjugated diolefin monomer to produce neodymium-aluminum catalyst component, and (2) subsequently reacting the neodymium-aluminum catalyst component with an alkyl aluminum chloride to produce the neodymium catalyst system.

Claims (18)

1. A process for the synthesis of an isoprene-butadiene rubber which comprises copolymerizing (a) isoprene monomer or a substituted isoprene monomer and (b) 1,3-butadiene monomer in the presence of a neodymium catalyst system, wherein the neodymium catalyst system is prepared by (1) reacting a neodymium carboxylate with an organoaluminum compound in the presence of a conjugated diolefin monomer to produce neodymium-aluminum catalyst component, and (2) subsequently reacting the neodymium-aluminum catalyst component with an alkyl aluminum chloride to produce the neodymium catalyst system, wherein the neodymium catalyst is prepared at a temperature that is within the range of about −60° C. to about 150° C., wherein the organoaluminum compound is selected from the group consisting of trialkylaluminum compounds and dialkylaluminum hydride compounds, and wherein the molar ratio of isoprene monomer to neodymium ranges from about 5/1 to about 500/1.

2. The process as specified in claim 1 wherein the alkyl aluminum chloride is a dialkyl aluminum chloride, and wherein molar ratio of the dialkyl aluminum chloride to neodymium is within the range of about 0.5:1 to about 3.5:1.

3. The process as specified in claim 1 wherein the neodymium carboxylate is selected from the group consisting of neodymium octoate, neodymium neodecanoate, and neodymium 2-ethyl hexanoate.

4. The process as specified in claim 1 wherein the alkaline aqueous neutralizer solution is an aqueous solution of sodium bicarbonate.

5. A process for the synthesis of an isoprene-butadiene rubber which comprises copolymerizing (a) isoprene monomer or a substituted isoprene monomer and (b) 1,3-butadiene monomer in the presence of a neodymium catalyst system, wherein the neodymium catalyst system is prepared by (1) reacting a neodymium carboxylate with an organoaluminum compound in the presence of a conjugated diolefin monomer to produce neodymium-aluminum catalyst component, and (2) subsequently reacting the neodymium-aluminum catalyst component with an alkyl aluminum chloride to produce the neodymium catalyst system, wherein the polymerization is terminated by the addition of an alkaline aqueous neutralizer solution, and wherein the alkaline aqueous neutralizer solution has a pH within the range of 7.1 to 9.5.

6. The process as specified in claim 5 wherein the alkaline aqueous neutralizer solution has a pH within the range of 7.5 to 9.0.

7. The process as specified in claim 5 wherein the alkaline aqueous neutralizer solution has a pH within the range of 8.0 to 8.5.

8. The process as specified in claim 5 wherein from 30 weight percent to 70 weight percent isoprene is copolymerized with 30 weight percent to 70 weight percent 1,3-butadiene.

9. The process as specified in claim 5 wherein the neodymium catalyst is prepared at a temperature that is within the range of about −60° C. to about 150° C.

10. The process as specified in claim 9 wherein the polymerization is carried out at a temperature within the range of about 10° C. to about 130° C. in an organic solvent.

11. The process as specified in claim 9 wherein said organoaluminum compound is selected from the group consisting of diethylaluminum hydride, di-n-propylaluminum hydride, di-n-butylaluminum hydride, diisobutylaluminum hydride, diphenylaluminum hydride, di-p-tolylaluminum hydride, dibenzylaluminum hydride, phenylethylaluminum hydride, phenyl-n-propylaluminum hydride, p-tolyethylalumin hydride, p-tolyl-n-propylaluminum hydride, p-tolylisopropylaluminum hydride, benzylethylaluminum hydride, benzyl-n-propylaluminum hydride, benzylisopropylaluminum hydride, ethylaluminum dihydride, butylaluminum dihydride, isobutylaluminum dihydride, octylaluminum dihydride, amylaluminum dihydride, trimethylaluminum, triethylaluminum, tri-n-propylaluminum, triisopropylaluminum, tri-n-propylaluminum, triisopropylaluminum, tri-n-butylaluminum, triisobutylaluminum, tripentylaluminum, trihexylaluminum, trioctylaluminum, triphenylaluminum, tri-p-tolyaluminum, tribenylaluminum, ethyldiphenylaluminum, ethyl-di-p-tolylaluminum, ethyldibenzylaluminum, diethylphenylaluminum, diethyl-p-tolylaluminum, and diethylbenzylaluminum.

12. The process as specified in claim 11 wherein the alkyl aluminum chloride is a dialkyl aluminum chloride, and wherein the dialkyl aluminum chloride is selected from the group consisting of dimethyl aluminum chloride, diethylaluminum chloride, dipropylaluminum chloride, dihexylaluminum chloride, diisobutylaluminum chloride, and didodecyaluminum chloride.

13. The process as specified in claim 9 wherein the mole ratio of the organoaluminum compound to the neodymium carboxylate is within the range of about 4/1 to about 200/1.

14. The process as specified in claim 13 wherein the neodymium catalyst is prepared at a temperature which is within the range of about 5° C. to about 15° C.

15. The process as specified in claim 9 wherein the organoaluminum compound is selected from the group consisting of trialkylaluminum compounds and dialkylaluminum hydride compounds.

16. The process as specified in claim 15 wherein the mole ratio of the organoaluminum compound to the neodymium carboxylate is within the range of about 10/1 to about 50/1.

17. A process for the synthesis of an isoprene-butadiene rubber which comprises copolymerizing (a) isoprene monomer or a substituted isoprene monomer and (b) 1,3-butadiene monomer in the presence of a neodymium catalyst system, wherein the neodymium catalyst system is prepared by (1) reacting a neodymium carboxylate with an organoaluminum compound in the presence of a conjugated diolefin monomer to produce neodymium-aluminum catalyst component, and (2) subsequently reacting the neodymium-aluminum catalyst component with an alkyl aluminum chloride to produce the neodymium catalyst system, where from 40 weight percent to 60 weight percent isoprene is copolymerized with 40 weight percent to 60 weight percent 1,3-butadiene.

18. The process as specified in claim 17 where from 45 weight percent to 55 weight percent isoprene is copolymerized with 45 weight percent to 55 weight percent 1,3-butadiene.

Assignments (4)
SECURITY INTEREST Recorded Dec 10, 2025
From: G-3 CHICKADEE PURCHASER, LLC
To: MIZUHO BANK, LTD., AS ADMINISTRATIVE AGENT
Reel/Frame 073900/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2025
From: THE GOODYEAR TIRE & RUBBER COMPANY
To: G-3 CHICKADEE PURCHASER, LLC
Reel/Frame 073591/0677 →
SECURITY INTEREST Recorded Oct 31, 2025
From: G-3 CHICKADEE PURCHASER, LLC
To: FORTRESS CREDIT CORP., AS ADMINISTRATIVE AGENT
Reel/Frame 073439/0048 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2021
From: SPILKER, THOMAS FRANKLIN
To: THE GOODYEAR TIRE & RUBBER COMPANY
Reel/Frame 054828/0225 →
Continuity (2)
Provisional Application 62951197 · Dec 20, 2019
Related Publication 20210189040A1 · Jun 24, 2021
Cited By (1)
US 12,649,811