IP Library Granted Patent US 11,208,511
Granted Patent B2
US 11,208,511 · App. 16/648,580 · Granted Dec 28, 2021

Non-random isobutylene copolymers

Inventors: André M. Gobin (Pearland, TX); Rajeev Kumar (Houston, TX); George Pappas (Galveston, TX); James A. Hopson (Humble, TX); Michael O. Nutt (Pearland, TX); Peggy J. Macatangay (League City, TX); Randall V. Redd (Spring, TX)
Assignee: TPC Group LLC
C08F210/12C08F2/001C08F2/01C08F4/14C08F212/08C08F236/08
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Quick Facts
Patent No.
US 11,208,511
App. No.
16/648,580
Granted
Dec 28, 2021
Kind
B2
Abstract

Non-random isobutylene copolymer includes repeat units derived from isobutylene and one or more comonomers selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, and C4 to C10 dienes other than isoprene, butadiene, limonene, cyclopentadiene, or dicyclopentadiene, wherein the molar ratio of isobutylene derived repeat units to the comonomer derived repeat units is from 75:1 to 1.5:1. The non-random copolymers have a molecular weight, Mn, of from 200 to 20,000 Daltons and typically have a high double bond content and a high vinylidene double bond content when diene monomers are utilized.

Claims (29)

1. A method of making a non-random isobutylene copolymer comprising:

(a) providing a reaction mixture to a first reactor comprising isobutylene monomer as well as a Lewis acid polymerization catalyst;

(b) polymerizing the reaction mixture in the first reactor while maintaining the first reactor at a temperature above −30° C. and utilizing a first reactor residence time of less than 45 minutes to polymerize at least 30% of the isobutylene monomer fed to the first reactor to produce an isobutylene prepolymer in a polymerization mixture;

(c) feeding the polymerization mixture to a second reactor along with a comonomer selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, piperylene and C4 to C10 dienes other than isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene or piperylene and optionally additional Lewis acid polymerization catalyst, wherein the molar ratio of isobutylene monomer fed to the first and second reactors to the comonomer is from 60:1 to 1:1;

(d) polymerizing the polymerization mixture and comonomer in the second reactor while maintaining the reactor at a temperature above −30° C. and utilizing a reactor residence time of less than 45 minutes to produce a non-random crude isobutylene copolymer in a copolymerization mixture; and

(e) recovering a purified non-random isobutylene copolymer from the copolymerization mixture having a molecular weight, Mn, of from 200 to 20,000 Daltons.

2. The method according to claim 1 , wherein the first and second reactors are selected from loop reactors, CSTRs and plug flow reactors.

3. A method of making a non-random isobutylene copolymer comprising:

(a) feeding a pre-formed isobutylene homopolymer or oligomer having from 2 to 40 repeat units to a reactor along with a comonomer selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, piperylene and C4 to C10 dienes other than isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene or piperylene and optionally additional Lewis acid polymerization catalyst and a diluent;

(b) polymerizing the polymer and comonomer mixture in the reactor while maintaining the reactor at a temperature above −30° C. and utilizing a reactor residence time of less than 45 minutes to produce a non-random crude isobutylene copolymer in a copolymerization mixture; and

(c) recovering a purified non-random isobutylene copolymer from the copolymerization mixture having a molecular weight, Mn, of from 200 to 20,000 Daltons;

wherein the molar ratio of isobutylene repeat units to comonomer repeat units in the non-random copolymer is from 60:1 to 1:1.

4. The method according to claim 1 , wherein the reactor(s) are maintained at a temperature of 0° C. or above.

5. The method according to claim 4 , wherein the reactor(s) are maintained at a temperature of 5° C. or above.

6. The method according to claim 1 , utilizing reactor residence times of 20 minutes or less.

7. The method according to claim 1 , wherein the conversion of comonomer is from 45% to 80%.

8. The method according to claim 1 , wherein the Lewis Acid polymerization catalyst comprises BF 3 and an alcohol co-catalyst.

9. The method according to claim 1 , wherein the molar ratio of isobutylene to the one or more comonomers added to the system is from 12:1 to 1:1.

10. The method according to claim 1 , wherein the purified non-random isobutylene copolymer has a molecular weight, Mn, of from 200 to 3000 Daltons.

11. The method according to claim 1 , wherein the comonomer is a diene monomer and the purified non-random isobutylene copolymer has, on average, from 1.25 to 5 double bonds per molecule.

12. The method according to claim 1 , wherein the comonomer is a diene monomer and the purified non-random isobutylene copolymer has, on average, from 0.85 to 2 vinylidene double bonds per molecule.

13. The method according to claim 1 , wherein the comonomer is a diene monomer and the purified non-random isobutylene copolymer has, on average, from 1.2 to 1.8 vinylidene double bonds per molecule.

14. An isobutylene non-random copolymer comprising repeat units derived from isobutylene and a comonomer selected from isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes, piperylene and C4 to C10 dienes other than isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene or piperylene, characterized in that the non-random copolymer exhibits a Tg at least 3.5° C. lower than a like random copolymer polymerized from the same monomer composition.

15. The isobutylene non-random copolymer according to claim 14 , wherein the non-random copolymer exhibits a Tg of from 3.5° C. to 20° C. lower than a like random copolymer polymerized from the same monomer composition.

16. The isobutylene non-random copolymer according to claim 14 , wherein the comonomer comprises isoprene.

17. The isobutylene non-random copolymer according to claim 14 , wherein the comonomer comprises para methyl styrene or alpha methyl styrene.

18. The isobutylene non-random copolymer according to claim 14 , wherein the comonomer comprises butadiene, cyclopentadiene, dicyclopentadiene, limonene, substituted styrenes other than alpha or para methyl styrenes, piperylene and C4 to C10 dienes other than isoprene, butadiene, cyclopentadiene, dicyclopentadiene, limonene or piperylene.

19. The isobutylene non-random copolymer according to claim 14 , wherein the molar ratio of isobutylene-derived repeat units to the comonomer-derived repeat units is from 30:1 to 3:1.

20. The isobutylene non-random copolymer according to claim 14 , wherein the molar ratio of isobutylene-derived repeat units to the comonomer-derived repeat units is from 12.5:1 to 3:1.

Assignments (15)
RELEASE OF SECURITY INTEREST Recorded Dec 16, 2024
From: GLAS TRUST COMPANY LLC
To: TPC GROUP LLC
Reel/Frame 069602/0182 →
SECURITY INTEREST Recorded Dec 16, 2024
From: TPC GROUP LLC
To: JEFFERIES FINANCE LLC, AS AGENT
Reel/Frame 069594/0055 →
TERMINATION AND RELEASE OF SUPPLEMENTAL GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 056447/0761 Recorded Dec 20, 2022
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS SUCCESSOR COLLATERAL AGENT TO U.S. BANK NATIONAL ASSOCIATION
To: TPC GROUP LLC
Reel/Frame 062171/0726 →
TERMINATION AND RELEASE OF GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 060287/0820 Recorded Dec 20, 2022
From: GLAS AMERICAS LLC, AS COLLATERAL AGENT
To: TPC GROUP LLC
Reel/Frame 062171/0674 →
TERMINATION AND RELEASE OF SUPPLEMENTAL GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS AT REEL/FRAME 055119/0158 Recorded Dec 20, 2022
From: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS SUCCESSOR COLLATERAL AGENT TO U.S. BANK NATIONAL ASSOCIATION
To: TPC GROUP LLC
Reel/Frame 062171/0666 →
RELEASE OF SECURITY INTEREST AT REEL/FRAME 60113/0169 Recorded Dec 16, 2022
From: ECLIPSE BUSINESS CAPITAL LLC, AS AGENT
To: TPC GROUP LLC
Reel/Frame 062142/0523 →
SECURITY INTEREST Recorded Dec 16, 2022
From: TPC GROUP LLC
To: ECLIPSE BUSINESS CAPITAL LLC, AS COLLATERAL AGENT
Reel/Frame 062130/0001 →
SECURITY INTEREST Recorded Dec 16, 2022
From: TPC GROUP LLC
To: GLAS TRUST COMPANY LLC, AS COLLATERAL AGENT
Reel/Frame 062130/0137 →
RELEASE OF SECURITY INTEREST AT REEL/FRAME 56544/0168 Recorded Jun 8, 2022
From: BANK OF AMERICA, N.A., AS AGENT
To: TPC GROUP LLC
Reel/Frame 060307/0988 →
GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Jun 6, 2022
From: TPC GROUP LLC
To: GLAS AMERICAS LLC, AS COLLATERAL AGENT
Reel/Frame 060287/0820 →
SECURITY INTEREST Recorded Jun 6, 2022
From: TPC GROUP LLC
To: ECLIPSE BUSINESS CAPITAL LLC, AS AGENT
Reel/Frame 060113/0169 →
SUPPLEMENTAL GRANT OF SECURITY INTEREST IN UNITED STATES PATENTS Recorded Jun 10, 2021
From: TPC GROUP LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 056544/0168 →
SUPPLEMENTAL PATENT SECURITY AGREEMENT Recorded Jun 1, 2021
From: TPC GROUP LLC
To: U.S. BANK NATIONAL ASSOCIATION
Reel/Frame 056447/0761 →
SECURITY INTEREST Recorded Feb 2, 2021
From: TPC GROUP LLC
To: U.S. BANK NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 055119/0158 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2020
From: GOBIN, ANDRÉ M; KUMAR, RAJEEV; PAPPAS, GEORGE; HOPSON, JAMES A; NUTT, MICHAEL O; MACATANGAY, PEGGY J; REDD, RANDALL V
To: TPC GROUP LLC
Reel/Frame 052209/0626 →