Controlled architecture polymerization with photoinitiator groups in backbone

• US 10,640,595 B2
• Filed: 10/25/2017
• Issued: 05/05/2020
• Est. Priority Date: 10/25/2016
• Status: Active Grant

• Current Assignee: Avery Dennison Corporation
• Original Assignee: Avery Dennison Corporation
• Inventors: Bartholomew, Eric L., Bottorf, William L., Heimbach, Kyle R., Miller, Brandon S., Waterman, Michael T., Zajaczkowski, Michael
• Primary Examiner(s): Mullis, Jeffrey C
• Application Number:
  US15/793,449
• Publication Number:
  US 20180112021A1
• Time in Patent Office: 923 Days
• CPC Class Codes: C08F 220/1804 C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
• CPC Class Codes: C08F 220/1808 C8-(meth)acrylate, e.g. isooctyl (meth)acrylate or 2-ethylhexyl (meth)acrylate
• CPC Class Codes: C08F 2438/02 Stable Free Radical Polymerisation [SFRP]; Nitroxide Mediated Polymerisation [NMP] for, e.g. using 2,2,6,6-tetramethylpiperidine-1-oxyl [TEMPO]
• CPC Class Codes: C08F 293/005 using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
• CPC Class Codes: C09J 153/00 Adhesives based on block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
• CPC Class Codes: C09J 7/387 Block-copolymers

Abstract

Acrylic copolymers that include the controlled placement of particular functional groups within the polymer structure are provided. The copolymers comprise a first reactive segment of including a functional group selected from the group consisting of a UV active functional group, a reactive functional group, a non-reactive functional group, and combinations thereof and a second segment including a functional group selected from the group consisting of a reactive functional group, a non-reactive functional group, and combinations thereof. The acrylic copolymers are manufactured via a controlled radical polymerization process. The copolymers are useful in the manufacture of adhesives and elastomers.

Claims

1. 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 UV active functional group, a reactive functional group, a non-reactive functional group, and combinations thereof; and

a second segment of controlled molecular weight and position that comprises at least one monomer comprising a functional group selected from the group consisting of a reactive functional group, a non-reactive functional group, and combinations thereof,

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

wherein the first reactive segment and the second segment are molecularly miscible before cure as expressed by their properties on the bulk state that are indicative of a single phase polymer.

2. The acrylic polymer of claim 1 wherein the first reactive segment comprises at least one monomer comprising a UV active functional group, and at least one monomer comprising a non-reactive functional group.

3. The acrylic polymer of claim 1 wherein the first reactive segment comprises at least one monomer comprising a UV active functional group and at least one monomer comprising a non-reactive functional group.

4. The acrylic polymer of claim 1 wherein the second segment comprises at least one monomer comprising a reactive functional group and at least one monomer comprising a non-reactive functional group.

5. The acrylic polymer of claim 1 wherein the second segment comprises at least one monomer comprising a non-reactive functional group.

6. The acrylic polymer of claim 1 wherein the first reactive segment comprises at least one monomer comprising a non-reactive functional group and at least one polymerizable comonomer comprising a crosslinkable functionality, the crosslinkable functionality selected from the group consisting of a UV active functional group, a reactive functional group, and combinations thereof.

7. The acrylic polymer of claim 1 wherein the first reactive segment comprises at least one monomer comprising a non-reactive functional group and at least one polymerizable comonomer comprising a crosslinkable functionality, the crosslinkable functionality is a UV crosslinkable functional group.

8. The acrylic polymer of claim 1 wherein the at least one monomer comprising non-reactive functional group within the first reactive segment is the same monomer comprising a non-reactive functional group present in the second segment.

9. The acrylic polymer of claim 1 wherein the at least one monomer comprising a reactive functional group within the first reactive segment is the same monomer comprising a reactive functional group present in the second segment.

10. The acrylic polymer of claim 1 wherein the at least one monomer comprising a reactive functional group comprises at least one monomer derived from the formula (II):

11. The acrylic polymer of claim 1 wherein the at least one monomer comprising a non-reactive functional group comprises at least one monomer derived from the formula (I):

12. The acrylic polymer of claim 1 wherein the at least one monomer comprising a non-reactive functional group is derived from C₁ to about C₂₀ alkyl, aryl, or cyclic acrylates or C₁ to about C₂₀ alkyl, aryl, or cyclic methacrylates.

13. The acrylic polymer of claim 1 wherein the first reactive segment comprises about 40% to about 99% by weight of the at least one monomer comprising a non-reactive functional group.

14. The acrylic polymer of claim 1 wherein the at least one monomer comprising a UV active functional group is about 10% or less by weight of the total polymer weight.

15. The acrylic polymer of claim 1 wherein the second segment is non-reactive with the UV active functional group and/or the reactive functional group.

16. The acrylic polymer of claim 1 wherein the at least one monomer comprising a non-reactive functional group is non-reactive with the UV active functional group and/or the reactive functional group.

17. The acrylic polymer of claim 1 wherein the first reactive segment and the second segment are positioned adjacent to the polymer chain ends.

18. The acrylic polymer of claim 1 wherein the reactive functional groups and/or the non-reactive functional groups are randomly spaced apart along the length of the polymer chain.

19. The acrylic polymer of claim 1 wherein the first reactive segment comprises 40% or less of the total polymer molecular weight.

20. The acrylic polymer of claim 1 wherein the acrylic polymer is a single phase polymer at room temperature.

21. The acrylic polymer of claim 1 wherein the acrylic polymer is a single phase polymer prior to crosslinking.

22. The acrylic polymer of claim 1 wherein the acrylic polymer is a single phase liquid polymer at room temperature.

23. The acrylic polymer of claim 1 wherein the acrylic polymer is a single phase liquid polymer prior to crosslinking.

24. The acrylic polymer of claim 1 wherein the acrylic polymer is a liquid polymer at room temperature.

25. The acrylic polymer of claim 1 wherein the acrylic polymer is a liquid polymer prior to crosslinking.

26. The acrylic polymer of claim 1 wherein the acrylic polymer is a homogeneous polymer at room temperature.

27. The acrylic polymer of claim 1 wherein the acrylic polymer is a homogeneous polymer prior to crosslinking.

28. The acrylic polymer of claim 1 wherein the acrylic polymer is a homogeneous liquid polymer prior to crosslinking.

29. The acrylic polymer of claim 1 wherein the acrylic polymer is a homogeneous liquid polymer at room temperature.

30. The acrylic polymer of claim 1 wherein the acrylic polymer exhibits no heterogeneity prior to crosslinking.

31. The acrylic polymer of claim 1 wherein the acrylic polymer exhibits no heterogeneity at room temperature.

32. The acrylic polymer of claim 1 wherein the glass transition temperature (Tg) of the acrylic polymer is within a range of from about 15°

C. to about −

115°

C.

33. The acrylic polymer of claim 1 wherein the UV active functional group is selected from the group consisting of benzophenones, double bonds, and combinations thereof.

34. The acrylic polymer of claim 1 wherein the UV active functional group is a benzophenone.

35. The acrylic polymer of claim 1 wherein the UV active functional group is represented by Formula (III) as follows:

36. The acrylic polymer of claim 35 wherein R₁ and R₂ is each independently an aromatic or substituted aromatic group.

37. The acrylic polymer of claim 35 wherein R₁ and R₂ is each independently a phenyl or substituted phenyl group.

38. The acrylic polymer of claim 1 wherein the UV active functional group is selected from the group consisting of acetophenone, an acetophenone derivative, benzophenone, a benzophenone derivative, anthraquinone, an anthraquinone derivative, benzile, a benzile derivative, thioxanthone, a thioxanthone derivative, xanthone, a xanthone derivative, a benzoin ether, a benzoin ether derivative, an alpha-ketol, an alpha-ketol derivative, and combinations thereof.

39. The acrylic polymer of claim 1 wherein the reactive functional group is 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.

40. The acrylic polymer of claim 1 wherein the reactive functional group is an acid.

41. The acrylic polymer of claim 1 wherein the acrylic polymer has a polydispersity greater than 3.0.

42. The acrylic polymer of claim 1 wherein the acrylic polymer has a number average molecular weight (Mn) within a range of from about 5,000 g/mol to about 150,000 g/mol.

43. The acrylic polymer of claim 1 comprising two first reactive segments A and one second segment B.

44. The acrylic polymer of claim 43 wherein the segments A are positioned on either side of the middle segment B on the polymer chain to define an ABA structure.

45. The acrylic polymer of claim 1 comprising two second segments B and one first reactive segment A.

46. The acrylic polymer of claim 45 wherein the blocks B are positioned on either side of the middle block A on the polymer chain to define a BAB structure.

53. A pressure sensitive adhesive composition comprising:

the acrylic polymer of claim 1; and

a crosslinking agent.

54. The adhesive composition of claim 53 wherein the crosslinking agent is from about 0.05% to about 5% by weight of adhesive solids.

55. The adhesive composition of claim 53 wherein the crosslinking agent is activated using one of heat, actinic radiation, electron beam radiation, and a metal based catalyst.

56. The adhesive composition of claim 53 wherein the adhesive composition further comprises at least one agent selected from the group consisting of tackifiers, plasticizers, antioxidants, pH controllers, medicaments, bactericides, growth factors, wound healing components, deodorants, perfumes, antimicrobials, fungicides, cutting agents, pigments, filler, diluents, flame retardants, and combinations thereof.

57. The adhesive composition of claim 53 wherein the weight percentage of solids is greater than 50%.

58. The adhesive composition of claim 53 wherein the adhesive exhibits an elastic/storage modulus (G′

) of less than the Dahlquist criterion value of 3×

10⁶ dynes/cm² (3×

10⁵ Pa) at room temperature.

59. The adhesive composition of claim 53 wherein the glass transition temperature (Tg) of the adhesive composition is within a range of from about 15°

C. to about −

115°

C.

63. An adhesive article comprising:

a substrate; and

the adhesive of claim 53 disposed on the substrate.

64. The adhesive article of claim 63 wherein the article is in the form of a tape.

47. 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 UV active functional group, a reactive functional group, a non-reactive functional group, and combinations thereof; and

a second segment of controlled molecular weight and position that comprises at least one monomer comprising a functional group selected from the group consisting of a reactive functional group, a non-reactive functional group, and combinations thereof,

wherein the first reactive segment and the second segment comprise a copolymer derived from (i) at least one monomer comprising a non-reactive functional group and (ii) at least one polymerizable comonomer comprising a crosslinkable functionality,

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

wherein the first segment and the second segment are molecularly miscible before cure as expressed by their properties in the bulk state that are indicative of a single phase polymer.

48. The acrylic polymer of claim 47 wherein the at least one monomer comprising a non-reactive functional group within the first reactive segment is the same monomer comprising a non-reactive functional group present in the second segment.

49. The acrylic polymer of claim 47 wherein the acrylic polymer is a homogeneous polymer prior to crosslinking.

50. The acrylic polymer of claim 47 wherein the first reactive segment comprises 40% or less of the total polymer molecular weight.

51. The acrylic polymer of claim 47 wherein the at least one monomer comprising a UV active functional group is about 10% or less by weight of the total polymer weight.

52. The acrylic polymer of claim 47 wherein the first reactive segment comprises about 40% to about 99% by weight of the at least one monomer comprising a non-reactive functional group.

60. 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 UV active functional group, a reactive functional group, a non-reactive functional group, and combinations thereof to thereby form a first reactive segment of controlled molecular weight and position;

polymerizing using a controlled radical polymerization process at least one monomer comprising a functional group selected from the group consisting of a reactive functional group, a non-reactive functional group, and combinations thereof to thereby form a second segment of controlled molecular weight and position;

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

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

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

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

61. The method of claim 60 wherein at least one of the first reactive segment and the second segment is polymerized in the presence of a RAFT agent.

62. The method of claim 60 wherein at least one of the first reactive segment and the second segment is polymerized in the presence of an SFRP agent.

65. An acrylic polymer consisting of:

at least one acrylic block copolymer comprising

a first reactive segment of controlled molecular weight and position consisting of at least one monomer comprising a UV active functional group, at least one monomer comprising a reactive functional group, and at least one monomer comprising a non-reactive functional group; and

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

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

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

66. The acrylic polymer of claim 65 wherein the first reactive segment consists of at least one monomer comprising a non-reactive functional group and at least one polymerizable comonomer comprising a crosslinkable functionality, the crosslinkable functionality consisting of a UV crosslinkable functional group and a reactive functional group.

67. The acrylic polymer of claim 65 wherein the first reactive segment consists of a copolymer derived from one or more of the monomers of the second segment and at least one polymerizable comonomer comprising a crosslinkable functionality, the crosslinkable functionality consisting of a UV crosslinkable functional group and a reactive functional group.

68. The acrylic polymer of claim 65 wherein the at least one monomer comprising a non-reactive functional group within the first reactive segment is the same monomer comprising a non-reactive functional group present in the second segment.

69. The acrylic polymer of claim 65 wherein the acrylic polymer is a homogeneous polymer prior to crosslinking.

70. The acrylic polymer of claim 65 wherein the first reactive segment is about 40% or less of the total polymer molecular weight.

71. The acrylic polymer of claim 65 wherein the at least one monomer comprising a UV active functional group is about 10% or less by weight of the total polymer weight.

72. The acrylic polymer of claim 65 wherein the first reactive segment comprises about 40% to about 99% by weight of the at least one monomer comprising a non-reactive functional group.

73. A pressure sensitive adhesive composition consisting of:

the acrylic polymer of claim 65; and

a crosslinking agent.

74. The adhesive composition of claim 73 wherein the crosslinking agent is from about 0.05% to about 5% by weight of adhesive solids.