Method for producing polydienes with reduced cold flow

Patent metadata

Field	Value
Publication number	US-12091474-B2
Application number	US-202017426941-A
Country	US
Kind code	B2
Filing date	Jan 28, 2020
Priority date	Jan 29, 2019
Publication date	Sep 17, 2024
Grant date	Sep 17, 2024

Abstract

A process for preparing a polydiene having increased viscosity and reduced cold flow that includes polymerizing a conjugated diene monomer in the presence of a lanthanide-containing compound to form an intermediate polymer, and then adding a non-organometallic trimellitate ester compound as a coupling agent to raise the viscosity of the intermediate polymer. The coupling agent is added to the intermediate polymer mixture in an amount of about 0.01 to about 0.15 parts per hundred monomer (phm) of the starting monomer amount.

First claim

The invention claimed is:

1. A process for preparing a polydiene, the process comprising the steps of:
a. polymerizing conjugated diene monomer to a conversion of 60 percent or more within a liquid-phase polymerization mixture to form an intermediate polymer, the liquid-phase polymerization mixture comprising conjugated diene monomer, a lanthanide-containing compound and an alkylating agent, wherein the intermediate polymer comprises a base Mooney viscosity;
b. adding a non-organometallic aromatic triester compound as a coupling agent in an amount of about 0.02 to about 0.12 phm to the intermediate polymer, wherein the addition of the non-organometallic trimellitate ester compound increases the base Mooney viscosity of the intermediate polymer in the range of about 30 to about 80 percent.

2. The process of claim 1 , wherein the intermediate polymer of step (a) comprises a base cold flow value and the addition of the non-organometallic aromatic triester compound increases the base cold flow value of the intermediate polymer in the range of about 20 to about 50 percent.

3. The process of claim 1 , wherein the lanthanide-containing compound is a neodymium compound.

4. The process of claim 1 , wherein the non-organometallic aromatic triester compound is a compound of formula (1)

wherein R, R′ and R″ are independently selected from hydrocarbyl groups containing 1 to 20 carbons.

5. The process of claim 4 , wherein the non-organometallic aromatic trimester compound is selected from the group consisting of trimethyl 1,2,4-benzenetricarboxylate, triethyl 1,2,4-benzenetricarboxylate, tripropyl 1,2,4-benzenetricarboxylate, tributyl 1,2,4-benzenetricarboxylate, tripentyl 1,2,4-benzenetricarboxylate, trihexyl 1,2,4-benzenetricarboxylate, triheptyl 1,2,4-benzenetricarboxylate, tricyclohexyl 1,2,4-benzenetricarboxylate, trioctyl 1,2,4-benzenetricarboxylate, tri(2-ethylhexyl) 1,2,4-benzenetricarboxylate, trinonyl 1,14-benzenetricarboxylate, tridecyl 1,2,4-benzenetricarboxylate, tridodecyl 1,2,4-benzenetricarboxylate, butyldimethyl 1,2,4-benzenetricarboxylate, butyldiethyl 1,2,4-benzenetricarboxylate, tri-2-ethylhexyl trimellitate and triisononyl trimellitate.

6. The process of claim 1 , wherein the non-organometallic aromatic triester compound is a compound of formula (2)

wherein R, R′ and R″ are independently selected from hydrocarbyl groups containing 1 to 20 carbons.

7. The process of claim 6 , wherein the non-organometallic aromatic trimester compound is selected from the group consisting of trimethyl 1,2,3-benzenetricarboxylate, triethyl 1,2,3-benzenetricarboxylate, tripropyl 1,2,3-benzenetricarboxylate, tributyl 1,2,3-benzenetricarboxylate, tripentyl 1,2,3-benzenetricarboxylate, trihexyl 1,2,3-benzenetricarboxylate, triheptyl 1,2,3-benzenetricarboxylate, tricyclohexyl 1,2,3-benzenetricarboxylate, trioctyl 1,2,3-benzenetricarboxylate, tri(2-ethylhexyl) 1,2,3-benzenetricarboxylate, trinonyl 1,2,3-benzenetricarboxylate, tridecyl 1,2,3-benzenetricarboxylate, tridodecyl 1,2,3-benzenetricarboxylate, butyldimethyl 1,2,3-benzenetricarboxylate, butyldiethyl 1,2,3-benzenetricarboxylate, tri-2-ethylhexyl hemimellitate and triisononyl hemimellitate.

8. The process of claim 1 , wherein the non-organometallic aromatic triester compound is a compound of formula (3)

wherein R, R′ and R″ are independently selected from hydrocarbyl groups containing 1 to 20 carbons.

9. The process of claim 8 , wherein the non-organometallic aromatic trimester compound is selected from the group consisting of trimethyl 1,3,5-benzenetricarboxylate, triethyl 1,3,5-benzenetricarboxylate, tripropyl 1,3,5-benzenetricarboxylate, tributyl 1,3,5-benzenetricarboxylate, tripentyl 1,3,5-benzenetricarboxylate, trihexyl 1,3,5-benzenetricarboxylate, triheptyl 1,3,5-benzenetricarboxylate, tricyclohexyl 1,3,5-benzenetricarboxylate, trioctyl 1,3,5-benzenetricarboxylate, tri(2-ethylhexyl) 1,3,5-benzenetricarboxylate, trinonyl 1,3,5-benzenetricarboxylate, tridecyl 1,3,5-benzenetricarboxylate, tridodecyl 1,3,5-benzenetricarboxylate, butyldimethyl 1,3,5-benzenetricarboxylate, butyldiethyl 1,3,5-benzenetricarboxylate, tri-2-ethylhexyl trimesitate and triisononyl trimesitate.

10. The process of claim 1 , wherein the non-organometallic aromatic triester compound is added in an amount of about 0.035 to about 0.085 phm to the intermediate polymer and the amount of the lanthanide-containing compound is present in an amount from about 0.001 to about 2 mmol per 100 g of conjugated diene monomer.

11. A polydiene polymer prepared the process of claim 1 , wherein the polythene polymer has a Mooney viscosity in the range about 35 to about 45 (ML 1+4 ).

12. A process for preparing a polybutadiene, the process comprising the steps of:
a. polymerizing butadiene monomer in a reaction vessel in the presence of a lanthanide-containing compound and an alkylating agent to a conversion of 80 percent or more to form, an intermediate polymer;
b. transferring the intermediate polymer to a second reaction vessel;
c. adding a non-organometallic aromatic triester compound as a coupling agent in an amount of about 0.02 to about 0.12 phm to the polymer cement in the second reaction vessel to form a polybutadiene cement, wherein the polybutadiene cement comprises a Mooney viscosity in the range about 35 to about 45 (ML 1+4 ).

13. The process of claim 12 , wherein the non-organometallic aromatic triester compound is a trimellitate ester compound selected from the group consisting of tri-2-ethylhexyl trimellitate or triisononyl trimellitate.

14. The process of claim 12 , wherein the intermediate polymer transferred to the second reaction vessel comprises a Mooney viscosity in the range about 20 to about 30 (ML 1+4 ).

15. The process of claim 12 , wherein the step a further comprises a halogen-containing compound in the reaction vessel.

16. The process of claim 1 , wherein the non-organometallic aromatic triester compound is added prior to the conjugated diene monomer being polymerized to a conversion rate of 95 percent.

17. The process of claim 1 , wherein the intermediate polymer of step (a) comprises a base relaxation time (T80) and the addition of the the non-organometallic aromatic treister compound increases the base relaxation time (T80) of the intermediate polymer in the range of about 20 to about 50 percent, the relaxation time (T80) is measured by applying force ot the intermediate polymer which results in an angular twisting of the intermediate polymer and releasing the applied force to let the intermediate polymer relax and measuring the time it taskes for the intermediate polymer to relax back to 80 percent of its final Mooney viscosity value.

18. A process for preparing a polydiene, the process comprising the steps of:
a. polymerizing conjugated diene monomer to a conversion of 60 percent to 95 percent within a liquid-phase polymerization mixture to form an intermediate polymer, the liquid-phase of polymerization mixture comprising conjugated diene monomer, a lanthanide-containing compound and an alkylating agent, wherein the intermediate polymer comprises a base Mooney viscosity;
b. adding a non-organometallic aromatic triester compound as a coupling agent in an amount of about 0.02 to about 0.12 phm to the intermediate

Assignees

• Bridgestone Americas Tire Operations Llc

Inventors

• Kuhel Iii James J
• Roggeman David M

Classifications

• C08F136/00

  Homopolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds (C08F132/00 takes precedence) · CPC title

• C08K5/12

  of cyclic polycarboxylic acids · CPC title

• C08F4/545

  rare earths being present, e.g. triethylaluminium + neodymium octanoate · CPC title

• C08F2/44

  Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers · CPC title

• C08F2/06

  Organic solvent · CPC title