IP Library Granted Patent US 9,790,309
Granted Patent B2
US 9,790,309 · App. 14/488,824 · Granted Oct 17, 2017

Grafted telechelic polyisobutylenes possessing reactive functionality, processes for preparing the same and curable compositions comprising the same

Inventors: Laxmisha Sridhar (Monmouth Junction, NJ); Smita Shah (Edison, NJ); Andrew D. Messana (Newington, CT); Anthony F. Jacobine (Meriden, CT)
Assignee: Henkel IP & Holding GmbH
C08F269/00C08F8/14C08F290/042
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Quick Facts
Patent No.
US 9,790,309
App. No.
14/488,824
Granted
Oct 17, 2017
Kind
B2
Abstract

Disclosed are reactive functionalized, PIB grafted polymers having an architecture of one or more pendent polyisobutylene moieties grafted on to an organic backbone, wherein the backbone is not polyisobutylene and contains at least one telechelic, reactive functionality. Also a process for making the reactive functionalized, PIB grafted polymer s and curable compositions comprising the reactive functionalized, PIB grafted polymers.

Claims (48)

1. A reactive functionalized, PIB grafted polymer comprising:

an organic backbone Z, the backbone including one or more aliphatic groups, one or more aromatic groups, one or more heteroatoms or any combination thereof, wherein the backbone Z is not polyisobutylene; at least one reactive functionality terminal to the backbone; and at least two polyisobutylene groups Y pendant from the organic backbone Z,

wherein the polymer is represented by one of the following formulas;

wherein organic backbone Z has a linear chain structure having 1 to about 50 atoms selected from the group consisting of C, H, N, O and S;

each M is independently selected from a covalent bond or an organic structure having 1 to about 20 atoms selected from the group consisting of C, H, N, O and S;

X, X 1 , X 2 , X 3 and X 4 are each independently H or a reactive functionality selected from acrylate, methacrylate, acrylamide, allyl, styrenic, vinyl ether, maleimide and N-vinylamide, but at least one of X, X 1 , X 2 , X 3 and X 4 in any formula must be a reactive functionality;

Y is a polyisobutylene group;

L connects one polyisobutylene group to one atom of the Z organic backbone or one atom of the M portion and each L is independently selected from a covalent bond or an organic structure having 1 to about 30 atoms selected from the group consisting of C, H, N, O and S;

R1 and R2 are each independently selected organic segments having 1 to about 30 atoms selected from the group consisting of C, H, N, O and S;

m is an integer from 2-10; and

n is an integer from 1-10.

2. The polymer of claim 1 , having a weight average molecular weight (Mw) of about 1,000 to about 30,000.

3. The polymer of claim 1 , in liquid form at room temperature.

4. The polymer of claim 1 , represented by the formula;

wherein

X 1 and X 2 are each independently H or a reactive functionality selected from acrylate, methacrylate, acrylamide, allyl, styrenic, vinyl ether, maleimide and N-vinylamide, but at least one of X 1 and X 2 must be a reactive functionality.

5. The polymer of claim 4 , wherein both X 1 and X 2 comprise an independently selected reactive functionality.

6. The polymer of claim 4 , wherein X 1 and X 2 are each a reactive functionality independently selected from acrylate or methacrylate.

7. The polymer of claim 1 , represented by the formula;

(Y-L) m -Z-(M-X) n

wherein

each X is independently H or a reactive functionality selected from acrylate, methacrylate, acrylamide, allyl, styrenic, vinyl ether, maleimide and N-vinylamide but at least one X must be a reactive functionality; and

L connects the polyisobutylene group Y to one atom of the Z organic backbone and each L is independently selected from a covalent bond or a structure having 1 to about 30 atoms selected from the group consisting of C, H, N, O and S.

8. The polymer of claim 7 , wherein L is selected from a covalent bond, C 1-5 alkyl, a heteroatom, ester, thioester, amide, imide, cyclic imide, ketone, carboxyl, urethane, carbonate, urea and combinations thereof.

9. The polymer of claim 1 , represented by the formula;

wherein

each Y is a polyisobutylene group.

10. The polymer of claim 9 , wherein all of X 1 , X 2 , X 3 and X 4 comprise an independently selected reactive functionality.

11. The polymer of claim 9 , wherein all of X 1 , X 2 , X 3 and X 4 comprise an independently selected acrylate reactive functionality or methacrylate reactive functionality.

12. The polymer of claim 9 , wherein R1 and R2 are the same.

13. A curable composition comprising the polymer of claim 1 .

14. The curable composition of claim 13 , further comprising a cure-inducing component and a co-reactant component.

15. Cured reaction products of the curable composition of claim 13 .

16. A method of making the reactive functionalized, PIB grafted polymer of claim 1 , comprising:

providing polyisobutylenesuccinic anhydride;

providing at least compound selected from a diacrylate, a monomethacrylate, an acrylamide, an amino alcohol, an allyl substituted monomer and a vinyl ether;

optionally providing one or more of a solvent, a Lewis acid and a Lewis base; and

reacting the polyisobutylenesuccinic anhydride with the at least compound selected from a diacrylate, a monomethacrylate, an acrylamide, an amino alcohol and an allyl substituted monomer.

17. The polymer of claim 1 , wherein Z comprises one or more aliphatic groups, one or more aromatic groups, one or more heteroatoms or any combination thereof; and Z can include one or more of branching, pendant aliphatic groups, pendant aromatic groups and pendant heteroatoms.

18. The polymer of claim 1 comprising L, wherein Y consists of a polyisobutylene group and L is selected from a covalent bond, C 1-5 alkyl, ester, thioester, amide, imide, cyclic imide, ketone, carboxyl, urethane, carbonate, urea and combinations thereof.

19. A reactive functionalized, PIB grafted polymer selected from the following structures:

20. The polymer of claim 1 comprising R 1 and R 2 , wherein Y consists of a polyisobutylene group and R1 and R2 are each independently selected from the group consisting of one or more C1-30 alkyl, C6-10 aryl, one or more heteroatoms selected from N, O or S atoms, or any combination thereof.

21. The polymer of claim 1 , wherein:

the Z organic backbone is selected from the group consisting of one or more aliphatic groups, one or more aromatic groups, one or more heteroatoms or any combination thereof and Z can include one or more of branching, pendant aliphatic groups, pendant aromatic groups and pendant heteroatoms;

M is selected from the group consisting of a covalent bond, heteroatom, C1-10 alkyl, C6-10 aryl, amide, urethane, urea, C3-6 cycloaliphatic, C6-10 cycloaryl, polyether and combinations thereof, and M may include within that structure one or more linear, branched or cyclic portions, one or more saturated, unsaturated or aromatic portions, one or more substituents selected from carbonyl, amide, alkyl, C3-6 cycloalkyl, C6-10 cycloaryl, one or more N, O or S atoms, or any combination thereof;

Y consists of a polyisobutylene group;

L is selected from the group consisting of a covalent bond, C 1-5 alkyl, ester, thioester, amide, imide, cyclic imide, ketone, carboxyl, urethane, carbonate, urea and combinations thereof; and

R1 and R2 are each independently selected from the group consisting of one or more C1-30 alkyl, C6-10 aryl, one or more heteroatoms selected from N, O or S atoms, or any combination thereof.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2022
From: HENKEL IP & HOLDING GMBH
To: HENKEL AG & CO. KGAA
Reel/Frame 059357/0267 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2015
From: HENKEL CORPORATION
To: HENKEL US IP LLC
Reel/Frame 035049/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 27, 2015
From: HENKEL US IP LLC
To: HENKEL IP & HOLDING GMBH
Reel/Frame 035050/0378 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2014
From: SRIDHAR, LAXMISHA; SHAH, SMITA; MESSANA, ANDREW D.; JACOBINE, ANTHONY F.
To: HENKEL CORPORATION
Reel/Frame 033784/0904 →
Continuity (3)
Continuation PCTUS2013033637 · Mar 25, 2013
Provisional Application 61639485 · Apr 27, 2012
Related Publication 20150005453A1 · Jan 1, 2015