IP Library Granted Patent US 10,407,525
Granted Patent B2
US 10,407,525 · App. 15/426,207 · Granted Sep 10, 2019

Controlled architecture polymers

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Quick Facts
Patent No.
US 10,407,525
App. No.
15/426,207
Granted
Sep 10, 2019
Kind
B2
Abstract

Acrylic copolymers that include the controlled placement of particular functional groups within the polymer structure are provided. The copolymers contain at least two reactive segments and are manufactured via a controlled radical polymerization process. The copolymers are useful in the manufacture of adhesives and elastomers.

Claims (65)

1. An acrylic polymer comprising:

at least one acrylic block copolymer comprising

two first reactive segments A of controlled molecular weight and position comprising at least one monomer comprising a functional group selected from the group consisting of a self reactive functional group, a reactive functional group, and combinations thereof; and

one second reactive segment B of controlled molecular weight and position comprising at least one monomer comprising a reactive functional group,

wherein the first reactive segments A and the second reactive segment B comprise a copolymer derived from (i) one or more monomers comprising nonreactive functional groups and (ii) at least one polymerizable comonomer comprising crosslinkable functionality,

wherein the first reactive segments A comprises at least one monomer comprising a self reactive functional group,

wherein the self reactive functional group is selected from the group consisting of silyl, anhydrides, epoxies, alkoxymethylol, and cyclic ethers, and

wherein the segments A are positioned on either side of the middle segment B on the polymer chain to define an ABA structure.

2. The acrylic polymer of claim 1 wherein the self reactive functional group is an epoxy.

3. The acrylic polymer of claim 1 wherein the reactive functional group is selected from the group consisting of acids, hydroxyls, amines, and thiols.

4. The acrylic polymer of claim 3 wherein the reactive functional group is an acid.

5. The acrylic polymer of claim 1 wherein the polymer has a polydispersity of less than 4.0.

6. The acrylic polymer of claim 1 wherein the polymer has a polydispersity of less than 3.5.

7. The acrylic polymer of claim 1 wherein the polymer has a polydispersity of less than 3.0.

8. The acrylic polymer of claim 1 wherein the polymer has a polydispersity of less than 2.5.

9. The acrylic polymer of claim 1 wherein the polymer has a polydispersity of less than 2.0.

10. The acrylic polymer of claim 1 wherein the polymer has a number average molecular weight (Mn) within the range of from about 40,000 to about 150,000.

11. The acrylic polymer of claim 10 wherein the polymer has a number average molecular weight (Mn) within the range of from about 50,000 to about 110,000.

12. A pressure sensitive adhesive composition comprising:

at least one acrylic block copolymer comprising

two first reactive segments A of controlled molecular weight and position comprising at least one monomer comprising a functional group selected from the group consisting of a self reactive functional group, a reactive functional group, and combinations thereof; and

one second reactive segment B of controlled molecular weight and position comprising at least one monomer comprising a reactive functional group; and

a crosslinking agent,

wherein the first reactive segments A and the second reactive segment B comprise a copolymer derived from (i) one or more monomers comprising non reactive functional groups and (ii) at least one polymerizable comonomer comprising crosslinkable functionality,

wherein the first reactive segments A comprises at least one monomer comprising a self reactive functional group,

wherein the self reactive functional group is selected from the group consisting of silyl, anhydrides, epoxies, alkoxymethylol, and cyclic ethers, and

wherein the segments A are positioned on either side of the middle segment B on the polymer chain to define an ABA structure.

13. The adhesive composition of claim 12 further comprising:

at least one agent selected from the group consisting of pigments, fillers, plasticizers, diluents, antioxidants, tackifiers, polymeric additives, and combinations thereof.

14. A method of preparing a pressure sensitive adhesive composition comprising:

polymerizing using a controlled radical polymerization process at least one monomer comprising a functional group selected from the group consisting of a self reactive functional group, a reactive functional group, and combinations thereof to thereby form two first reactive segments A of controlled molecular weight and position;

polymerizing using a controlled radical polymerization process at least one monomer comprising a reactive functional group to thereby form one second reactive segment B of controlled molecular weight and position;

wherein at least one of the first reactive segments A and the second reactive segment B comprises an acrylate group;

forming an acrylic polymer from the first reactive segments A and the second reactive segment B;

crosslinking the acrylic polymer by mixing the acrylic polymer with an amount of a crosslinking agent;

wherein the first reactive segments A and the second reactive segment B comprise a copolymer derived from (i) one or more monomers comprising nonreactive functional groups and (ii) at least one polymerizable comonomer comprising crosslinkable functionality,

wherein the first reactive segments A comprises at least one monomer comprising a self reactive functional group,

wherein the self reactive functional group is selected from the group consisting of silyl, anhydrides, epoxies, alkoxymethylol, and cyclic ethers, and

wherein the segments A are positioned on either side of the middle segment B on the polymer chain to define an ABA structure.

15. The method of claim 14 wherein at least one of the first reactive segment and the second reactive segment is polymerized in the presence of a RAFT agent.

16. The method of claim 14 wherein at least one of the first reactive segment and the second reactive segment is polymerized in the presence of an SFRP agent.

17. The method of claim 14 further comprising the step of crosslinking the functional groups of the reactive segments.

18. The acrylic polymer of claim 1 wherein the one or more monomers comprising nonreactive functional groups are derived from acrylates, methacrylates, or mixtures thereof.

19. The acrylic polymer of claim 1 wherein the one or more monomers comprising nonreactive functional groups are derived from C 1 to about C 20 alkyl, aryl, or cyclic acrylates, C 1 to about C 20 alkyl, aryl, or cyclic methacrylates, or mixtures thereof.

20. The acrylic polymer of claim 1 wherein the first second reactive segment comprise at least one monomer comprising the formula (II):

where R 3 is H or CH 3 and R 4 is a branched or unbranched, saturated alkyl group comprising 4 to 14 carbon atoms.

21. The acrylic polymer of claim 1 wherein the first and second reactive segment comprise at least one monomer derived from the formula (I):

where R is H or CH 3 and X comprises a functional group capable of crosslinking,

wherein the functional group comprises at least one functional group selected from the group consisting of hydroxyl, carboxyl, carbonyl, carbonate ester, isocyanate, epoxy, vinyl, amine, amide, imide, anhydride, mercapto (thiol), acid, acrylamide, acetoacetyl groups, alkoxymethylol, cyclic ether groups, and combinations thereof.

22. The acrylic polymer of claim 1 wherein the first reactive segment and the second reactive segment are molecularly miscible before cure as expressed by their properties in the bulk state that are indicative of a single phase behavior.

23. The acrylic polymer of claim 1 wherein the one or more monomers comprising nonreactive functional groups is the same type of monomer present in both the first and second reactive segments.

24. An acrylic polymer comprising:

at least one acrylic block copolymer comprising two first reactive segments A of controlled molecular weight and position that comprises at least one monomer comprising a functional group selected from the group consisting of a self reactive functional group, a reactive functional group, and combinations thereof; and

one second reactive segments B of controlled molecular weight and position that comprises at least one monomer comprising a reactive functional group,

wherein the first reactive segments A comprises at least one monomer comprising a self reactive functional group, and

wherein the first reactive segments A and the second reactive segment B comprise a copolymer derived from (l) one or more monomers comprising nonreactive functional groups and (ii) at least one polyrnerizable comonorner comprising crosslinkable functionality,

wherein the reactive functional group is selected from the group consisting of acids, hydroxyls, amines, and thiols, and

Wherein the segments A are positioned on either side of the middle segment B on the polymer chain to define an ABA structure.

25. An acrylic polymer comprising:

at least one acrylic block copolymer comprising a first reactive segment of controlled molecular weight and position that comprises at least one monomer comprising a functional group selected from the group consisting of a self reactive functional group, a reactive functional group, and combinations thereof; and

a second reactive segment of controlled molecular weight and position that comprises at least one monomer comprising a reactive functional group,

wherein the first reactive segment and the second reactive segment comprise a copolymer derived from (i) one or more monomers comprising nonreactive functional groups and (ii) at least one polyrnerizable comonorner comprising crossiinkabie functionality,

wherein the first reactive segment and the second reactive segment are molecularly miscible before cure,

wherein the first reactive segment comprises at least one monomer comprising a self reactive functional group, and

wherein the self reactive functional group is selected from the group consisting of silyl, anhydrides, epoxies, alkoxymethylol, and cyclic ethers.

Assignments (1)
CHANGE OF CORPORATE ADDRESS Recorded Jul 22, 2022
From: AVERY DENNISON CORPORATION
To: AVERY DENNISON CORPORATION
Reel/Frame 060814/0274 →
Cited By (1)
US 12,630,751