Adhesive compositions for easy application and improved durability
View Patent ↗The present invention is directed to an adhesive composition comprising a crosslinkable acrylic copolymer, a multi-functionalized crosslinkable oligomer and a photoinitiator wherein the composition exhibits excellent wet out characteristics as reflected in a tan delta value of at least 0.5, preferably greater than 0.5, more preferable greater than 0.8 as measured at 20° C. resulting from a first curing stage, and improved stiffness and temperature resistance as reflected in a storage elastic modulus of at least 300,000 Pa at 20° C. and a shear adhesion failure temperature of at least 425° F. (218.3° C.) at 1 Kg/in 2 (0.155 Kg/cm 2 ), respectively, which result from a second sequential curing stage.
1. An adhesive composition comprising:
(a) a crosslinkable acrylic copolymer;
(b) a multi-functionalized crosslinkable oligomer; wherein the oligomer comprises a functional moiety selected from the group consisting of acrylate, epoxy, hydroxy, and combinations thereof;
(c) a photoinitiator which initiates polymerization of the oligomer and is present in an amount of between 0.1 to 5% by weight relative to the dry weight of the acrylic copolymer;
and
wherein the composition is free of a mono-functionalized oligomer and has:
(i) a first thermal curing stage wherein the acrylic copolymer is crosslinked with itself and the partially cured composition exhibits a tan δ value greater than 0.8 as measured at 20° C.; and
(ii) a second sequential radiation curing stage wherein the oligomer is crosslinked with itself and the fully cured composition exhibits a storage modulus value of at least 300,000 Pa at 20° C., a shear adhesion failure temperature of at least 425° F. (218.3° C.) at 1 Kg/in 2 (0.155 Kg/cm 2 ), a heated shear value at 160° C. of greater than 10,000 minutes and a peel force value of at least 3.2 lb/in.
2. The composition as defined in claim 1 wherein the acrylic copolymer is a solvent-borne or solvent-free acrylic copolymer.
3. The composition as defined in claim 1 wherein the acrylic copolymer is crosslinked during the first curing stage by evaporation of a solvent.
4. The composition as defined in claim 1 wherein the oligomer is present in an amount of between 5 to 40% by weight relative to the dry weight of the acrylic copolymer.
5. The composition as defined in claim 1 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of at least 200 nm.
6. The composition as defined in claim 1 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of between 300 to 500 nm.
7. The composition as defined in claim 1 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of between 320 to 440 nm.
8. The composition as defined in claim 1 wherein the fully cured composition exhibits a tan delta value of less than 0.8 as measured at 20° C. after the second curing stage.
9. The composition as defined in claim 1 wherein the fully cured composition exhibits a room temperature shear adhesion value of least 500 hours at 5 lb/in 2 (0.352 Kg/cm 2 ) after the second curing stage.
10. The composition as defined in claim 1 wherein the acrylic copolymer comprises a comonomer selected from the group consisting of acrylamide, acrylonitrile, acrylic acid, alpha-methyl styrene, butyl acrylate, ethyl acrylate, n-butyl acrylate, ethyl acrylate, 2-ethylhexyl acrylate, glycidylmethacrylate, 2-hydroxyethylmethacrylate, hexyl acrylate, hydroxyethyl acrylate, isobornyl acrylate, isobutyl acrylate, iso-octyl acrylate, isodecyl acrylate, isononyl acrylate, methacrylic acid, methyl acrylate, methacrylonitrile, n-vinyl caprolactam, nonyl acrylate, caprolactam, propyl acrylate, tert-butyl acrylate, vinyl acetate, vinyl pyrrlidone, styrene, and combinations thereof.
11. The composition as defined in claim 1 wherein the acrylic copolymer is a solvent-borne acrylic copolymer comprising 2-ethylhexyl acrylate and vinyl acetate comonomers.
12. The composition as defined in claim 1 further comprising a crosslinking agent which reacts with the solvent-borne or solvent-free acrylic copolymer.
13. The composition as defined in claim 12 wherein the crosslinking agent is selected from the group consisting of amino resins, aziridines, melamines, isocyanates, metal acid esters, metal chelates, multifunctional propylene imines, and polycarbodiimides.
14. The composition as defined in claim 12 wherein the crosslinking agent is selected from the group consisting of aluminum(III) acetylacetonate (AlAcAc), chromium(III) acetylacetonate (CrAcAc), iron(III) acetylacetonate (FeAcAc), cobalt(II) acetylacetonate (CoAcAc), nickel(II) acetylacetonate (NiAcAc), manganese(III) acetylacetonate (MnAcAc), titanium(IV) acetylacetonate (TiAcAc), zinc(II) acetylacetonate (ZnAcAc), zirconium(IV) acetylacetonate (ZrAcAc), and combinations thereof.
15. The composition as defined in claim 12 wherein the crosslinking agent is aluminum (III) acetylacetonate (AlAcAc).
16. The composition as defined in claim 1 wherein the functional moiety of the oligomer is acrylate.
17. The composition as defined in claim 1 wherein the functional moiety of the oligomer is epoxy.
18. The composition as defined in claim 1 wherein the oligomer comprises a monomer or comonomer selected from the group consisting of acrylate, acrylic, epoxy, polyether, polyol, polyester, saturated and unsaturated rubber, polyurethane and combinations thereof.
19. The composition as defined in claim 1 wherein the photoinitiator is selected from the group consisting of acetophenones, aryl phosphineoxides, aryl sulfonium and aryl iodonium salts of hexafluorophosphate, a mixture of benzyl/benzoin moieties, benzopheneones, thioxanthones, onium salts, and combination thereof.
20. An adhesive composition comprising:
(a) a crosslinkable acrylic copolymer comprising comonomers selected from the group consisting of ethyl acetate, 2-ethylhexyl acrylate, methyl acrylate, vinyl acetate and combinations thereof;
(b) a multi-functionalized crosslinkable oligomer comprising a functional moiety selected from the group consisting of acrylate, epoxy, hydroxy, and combinations thereof;
(c) a photoinitiator which initiates polymerization of the oligomer;
(d) a crosslinking agent which the acrylic copolymer; and
wherein the composition is free of a mono-functionalized oligomer and has:
(i) a first thermal curing stage wherein the acrylic copolymer is crosslinked with itself and the partially cured composition exhibits a tan δ value greater than 0.8 as measured at 20° C., and
(ii) a second sequential radiation curing stage wherein the oligomer is crosslinked with itself and the fully cured composition exhibits a storage modulus value of at least 300,000 Pa at 20° C., a shear adhesion failure temperature of at least 425° F. (218.3° C.) at 1 Kg/in 2 (0.155 Kg/cm 2 ), a heated shear value at 160° C. of greater than 10,000 minutes and a peel force value of at least 3.2 lb/in.
21. The composition as defined in claim 20 wherein the acrylic copolymer is a solvent-borne acrylic copolymer.
22. The composition as defined in claim 20 wherein the oligomer is present in an amount of between 5 to 40% by weight relative to the dry weight of the acrylic copolymer.
23. The composition as defined in claim 20 wherein the photoinitiator is present in an amount of between 0.5 to 5% by weight relative to the dry weight of the acrylic copolymer.
24. The composition as defined in claim 20 wherein the acrylic copolymer is crosslinked during the first curing stage by evaporation of a solvent.
25. The composition as defined in claim 20 wherein the crosslinking agent is selected from the group consisting of aluminum(III) acetylacetonate (AlAcAc), chromium(III) acetylacetonate (CrAcAc), iron(III) acetylacetonate (FeAcAc), cobalt(II) acetylacetonate (CoAcAc), nickel(II) acetylacetonate (NiAcAc), manganese(III) acetylacetonate (MnAcAc), titanium(IV) acetylacetonate (TiAcAc), zinc(II) acetylacetonate (ZnAcAc), zirconium(IV) acetylacetonate (ZrAcAc), and combinations thereof.
26. The composition as defined in claim 20 wherein the oligomer comprises a monomer or comonomer selected from the group consisting of acrylate, acrylic, epoxy, ether polyol, ester, saturated and unsaturated rubber, urethane and combinations thereof.
27. The composition as defined in claim 20 wherein the photoinitiator is selected from the group consisting of acetophenone, aryl phosphineoxides, aryl sulfonium and aryl iodonium salts of hexafluorophophate, a mixture of benzyl/benzoin moieties, benzophenone, thioxanthone, and combination thereof.
28. The composition as defined in claim 20 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of at least 200 nm.
29. The composition as defined in claim 20 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of between 320 to 440 nm.
30. The composition as defined in claim 20 wherein the fully cured composition exhibits a tan delta value of less than 0.8 as measured at 20° C. after the second curing stage.
31. The composition as defined in claim 20 wherein the fully cured composition exhibits a room temperature shear adhesion value of least 500 hours at 5 lb/in 2 (0.352 Kg/cm 2 ) after the second curing stage.
32. An adhesive composition comprising:
(a) a solvent-borne crosslinkable acrylic copolymer comprising comonomers selected from the group consisting of ethyl acetate, 2-ethylhexyl acrylate, methyl acrylate and vinyl acetate and combinations thereof;
(b) a multi-functionalized crosslinkable oligomer comprising two terminally positioned acrylate functional moieties and a urethane monomer or comonomer unit; wherein the oligomer is present in an amount of between 5 to 40% by weight relative to the dry weight of the acrylic copolymer;
(c) a photoinitiator which initiates polymerization of the oligomer and is present in an amount of between 0.5 to 5% by weight relative to the dry weight of the acrylic copolymer;
(d) a crosslinking agent which reacts with the acrylic copolymer; and
wherein the composition is free of a mono-functionalized oligomer and has:
(i) a first thermal curing stage wherein the acrylic copolymer is crosslinked with itself and the partially cured composition exhibits a tan δ value greater than 0.8 as measured at 20° C., and
(ii) a second sequential radiation curing stage wherein the oligomer is crosslinked with itself and the fully cured composition exhibits a storage modulus value of at least 300,000 Pa at 20° C., a shear adhesion failure temperature of at least 425° F. (218.3° C.) at 1 Kg/in 2 (0.155 Kg/cm 2 ), a heated shear value at 160° C. of greater than 10,000 minutes and a peel force value of at least 3.2 lb/in.
33. The composition as defined in claim 32 wherein the acrylic copolymer is crosslinked during the first curing stage by evaporation of a solvent.
34. The composition as defined in claim 32 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of at least 200 nm.
35. The composition as defined in claim 32 wherein the oligomer is crosslinked during the second curing stage by exposure to light having a wavelength of between 320 to 440 nm.
36. The composition as defined in claim 32 wherein the fully cured composition exhibits a tan delta value of less than 0.8 as measured at 20° C. after the second curing stage.
37. The composition as defined in claim 32 wherein the fully cured composition exhibits a room temperature shear adhesion value of least 500 hours at 5 lb/in 2 (0.352 Kg/cm 2 ) after the second curing stage.
38. The composition as defined in claim 32 wherein the photoinitiator is selected from the group consisting of acetophenone, aryl phosphineoxides, aryl sulfonium and aryl iodonium salts of hexafluorophophate, a mixture of benzyl/benzoin moieties, benzophenone, thioxanthone, and combinations thereof.
39. The composition as defined in claim 32 wherein the photoinitiator is an aryl phosphineoxide or aryl sulfonium or aryl iodonium salt of hexafluorophophate.
40. The composition as defined in claim 32 wherein the crosslinking agent is selected from the group consisting of aluminum(III) acetylacetonate (AlAcAc), chromium(III) acetylacetonate (CrAcAc), iron(III) acetylacetonate (FeAcAc), cobalt(II) acetylacetonate (CoAcAc), nickel(II) acetylacetonate (NiAcAc), manganese(III) acetylacetonate (MnAcAc), titanium(IV) acetylacetonate (TiAcAc), zinc(II) acetylacetonate (ZnAcAc), zirconium(IV) acetylacetonate (ZrAcAc), and combinations thereof.