Pressure sensitive adhesives possessing high load bearing capability

• US 6,677,402 B2
• Filed: 02/20/2002
• Issued: 01/13/2004
• Est. Priority Date: 10/07/1999
• Status: Expired due to Term

• Current Assignee: 3M Innovative Properties Company (3M Company)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: Heilmann, Steven M., Abuelyaman, Ahmed S., Gaddam, Babu N.
• Primary Examiner(s): MULLIS, JEFFREY C
• Application Number:
  US10/081,689
• Publication Number:
  US 20020132927A1
• Time in Patent Office: 692 Days
• Field of Search: 525/185, 525/190, 525/242, 525/452, 525/539, 525/540
• US Class Current: 525/185
• CPC Class Codes: C09J 201/02 characterised by the presence of specified groups , e.g. terminal or pendant functional groups
• CPC Class Codes: C09J 7/385 Acrylic polymers

Abstract

Pressure sensitive adhesives are provided which possess high load bearing capabilities at elevated temperatures. The adhesives are prepared by polymerization of a syrup polymer composition having a first solute polymer having reactive, pendant functional groups, a second component having co-reactive functional groups, and a monomer mixture. The syrup polymer contains reactive electrophilic or nucleophilic functional groups that can subsequently crosslink by reaction with a second component having co-reactive functional groups.

Claims

1. A syrup polymer composition comprising

a) a first component solute polymer comprising a plurality of polymerized monomer units comprising pendant reactive nucleophilic or electrophilic functional groups;

b) a second component dendritic polymer co-reactive with said first component solute polymer; and

c) a third component comprising at least one free-radically polymerizable solvent monomer.

2. The composition of claim 1 which comprises:

(a) from 2 to 20 parts by weight of said first component solute polymer;

(b) from 0.01 to 10.00 parts by weight of said second component dendritic polymer;

(c) from 70.00-97.99 parts by weight of said third component solvent monomer.

3. The composition of claim 1 having a viscosity of 500 to 10,000 cPs at 22°

C.

4. The composition of claim 1 wherein said first solute polymer comprises

(a) from 75.00 to 99.99 parts by weight of polymerized monomer units derived from acrylic acid esters of non-tertiary alkyl alcohols containing 1-14 carbon atoms;

(b) from 0.01 to 5.00 parts by weight of polymerized monomer units derived from of an ethylenically-unsaturated monomer having a reactive nucleophilic or electrophilic functional group;

(c) from 0 to 10 parts by weight of at least one polar monomer; and

(d) from 0 to 10 parts by weight of at least one other monomer.

5. The syrup polymer composition of claim 4 wherein said polar monomer, when present, is selected from the group consisting of substituted (meth)acrylamides, N-vinyl pyrrolidone, N-vinyl caprolactam, acrylonitrile, tetrahydrofurfuryl acrylate, acrylamides, and mixtures thereof.

6. The syrup polymer of claim 1 wherein said second component comprises a dendritic polymer having co-reactive functional groups and a functionality of greater than 3.

7. The composition of claim 6 wherein said dendritic polymer the general formula R-(Z)_n where Z is a functional group, n is greater than 3 and R is an organic radical having a valency of n.

8. The composition of claim 7 wherein said dendritic polymer is selected from the group consisting of a dendrimer, regular dendron, dendrigraft or hyperbranched polymer.

9. The composition of claim 1 wherein said third component solvent monomer comprises polymerizable, ethylenically-unsaturated monomers selected from acrylic acid esters of non-tertiary alkyl alcohols containing 1-14 carbon atoms.

10. The composition of claim 4, wherein said nucleophilic functional group of said ethylenically-unsaturated monomer possessing a nucleophilic functional group is selected from hydroxy, amino, isocyanato and azlactone functional groups.

11. A process for making a substrate bearing a coating of a crosslinkable pressure-sensitive adhesive on at least one surface thereof, comprising the steps of:

a) coating onto said substrate the syrup polymer composition of claim 1, and

b) subjecting said coated mixture to sufficient energy to activate said initiator and to polymerize said solvent monomer(s).

12. The process of claim 11 wherein said polymerization of said solvent monomers generates sufficient heat to crosslink said first solute polymer and second component by forming covalent bonds between said reactive groups of said first solute polymer and co-reactive groups of said second component.

13. The process of claim 11 wherein said syrup polymer composition has been partially polymerized to a coatable viscosity of from 750 to 7,500 cPs at 22°

C. prior to step a).

14. The process of claim 11 whereon said syrup polymer composition comprises:

(a) from 2 to 20 parts by weight of said first component solute polymer;

(b) from 0.01 to 10.00 parts by weight of said second component dendritic polymer;

(c) from 70.00 to 97.99 parts by weight of said third component solvent monomer, and

(d) from 0.0001 to about 3.0 parts by weight of a free-radical initiator.

15. The process of claim 11 wherein said first component solute polymer comprises:

(a) from 75.00 to 99.99 parts by weight of polymerized monomer units derived from acrylic acid esters of non-tertiary alkyl alcohols containing 1-14 carbon atoms;

(b) from 0.01 to 5.00 parts by weight of polymerized monomer units derived from of an ethylenically-unsaturated monomer having a reactive nucleophilic or electrophilic functional group;

(e) from 0 to 10 parts by weight of at least one polar monomer; and

(f) from 0 to 10 parts by weight of at least one other monomer.

16. The process of claim 15 wherein said polar monomer, when present, is selected from the group consisting of substituted (meth)acrylamides, N-vinyl pyrrolidone, N-vinyl caprolactam, acrylonitrile, tetrahydrofurfuryl acrylate, acrylamides, and mixtures thereof.

17. The process of claim 11 wherein said polyfunctional compound the general formula R-(Z)_n where Z is a functional group, n is greater than 3 and R is an organic radical having a valency of n.

18. The process of claim 11 wherein said wherein said dendritic polymer is selected from the group consisting of a dendrimer, regular dendron, dendrigraft or a hyperbranched polymer.

19. The process of claim 11 wherein said third component solvent monomer comprises polymerizable, ethylenically-unsaturated monomers selected from acrylic acid esters of non-tertiary alkyl alcohols containing 1-14 carbon atoms.

20. The process of claim 15 wherein said nucleophilic functional group of said ethylenically-unsaturated monomer possessing a nucleophilic functional group is selected from hydroxy, amino, isocyanato and azlactone functional groups.