Stress relaxation in crosslinked polymers
View Patent ↗The invention provides methods for inducing reversible chain cleavage of polymer chains in a crosslinked polymeric material. Reversible cleavage of the polymer backbone is capable of relieving stress in the polymeric material as the bonds reform in a less stressed state. The invention also provides methods for making polymeric materials capable of reversible chain cleavage, materials made by the methods of the invention, and linear monomers containing reversible chain cleavage groups which are useful in the materials and methods of the invention.
1. A mixture for forming a polymeric material comprising a crosslinked network of polymer chains, a plurality of the polymer chains incorporating an addition-fragmentation chain transfer functionality, the mixture comprising
a) a first monomer which is a linear multifunctional monomer containing an addition-fragmentation chain transfer functionality in the monomer backbone and a plurality of polymerizable groups;
b) a second monomer not containing an addition-fragmentation chain transfer functionality; and
c) a source of free radicals or cations.
2. The mixture of claim 1 , wherein the amount of the first monomer is selected so that the ratio of the number of reversible chain cleavage groups to the number of crosslinks in the crosslinked network is greater than or equal to one-quarter.
3. The mixture of claim 1 , wherein the first monomer is given by:
A 1 -Y-A 2
where A 1 and A 2 each comprise at least one polymerizable group and Y is the addition-fragmentation chain transfer functionality.
4. The mixture of claim 3 , wherein Y is an allyl sulfide.
5. The mixture of claim 3 , wherein Y is a RAFT agent.
6. The mixture of claim 3 , wherein Y is a dithiocarbamate.
7. The mixture of claim 3 , wherein Y is a trithiocarbonate.
8. The mixture of claim 3 , wherein Y is a thiuram disulfide.
9. The mixture of claim 3 , wherein the polymerizable groups of A 1 and A 2 are each selected from the group consisting of acrylates, methacrylates, oxiranes (epoxies), amines, vinyl ethers, vinylics, allyl ethers, allylics, thiols, styrenics, isocyanates, and hydroxides, and combinations thereof.
10. The mixture of claim 9 , wherein the polymerizable groups of A 1 and A 2 are each independently selected from the group consisting of acrylates, methacrylates, vinyl ethers and allyl ethers.
11. The mixture of claim 1 , wherein the second monomer is selected from the group consisting of ethylene oxides, ethylene glycols, vinyl acetates, vinyl pyrrolidones, ethyloxazolines, amino acids, saccharides, proteins, anhydrides, vinyl ethers, thiols, amides, carbonates, phenylene oxides, acetals, sulfones, phenylene sulfides, esters, fluoropolymers, imides, amide-imides, etherimides, ionomers, aryletherketones, olefins, styrenes, vinyl chlorides, ethylenes, acrylates, methacrylates, amines, phenols, acids, nitriles, acrylamides, maleates, benzenes, epoxies, cinnamates, azoles, silanes, chlorides, epoxides, lactones, isocyanates, hydroxides and amides.
12. The mixture of claim 11 , wherein the second monomer is an acrylate or a methacrylate.
13. The mixture of claim 1 , further comprising a third ring opening monomer containing an addition-fragmentation chain transfer functionality in the backbone.
14. The mixture of claim 1 , wherein a source of free radicals is provided in c), the source of free radicals being a photoinitiator, a thermal initiator, or a redox initiator.
15. The mixture of claim 1 , wherein the mixture further comprises a second source of radicals or cations different from the first.
16. The mixture of claim 1 , wherein the polymeric material is a coating material, a dental material, an optical material, or part of a fiber reinforced composite material.
17. A mixture for forming a polymeric material comprising a crosslinked network of polymer chains, a plurality of the polymer chains incorporating an addition-fragmentation chain transfer functionality, the mixture comprising
a) a first monomer comprising an addition-fragmentation chain transfer functionality and two polymerizable groups, the addition-fragmentation chain transfer functionality being linked to each of the two polymerizable groups by a C 1 -C 10 hydrocarbon chain optionally substituted with cyclic or aromatic groups;
b) a second monomer not containing an addition-fragmentation chain transfer functionality; and
c) a source of free radicals or cations.
18. The mixture of claim 17 , wherein the amounts of the first and second monomer are selected so that the ratio of the number of reversible chain cleavage groups to the number of crosslinks in the crosslinked network is greater than or equal to one-quarter.
19. The mixture of claim 17 , wherein the addition-fragmentation chain transfer functionality is an allyl sulfide.
20. The mixture of claim 17 , wherein the addition-fragmentation chain transfer functionality is a RAFT agent.
21. The mixture of claim 17 , wherein the addition-fragmentation chain transfer functionality is a dithiocarbamate.
22. The mixture of claim 17 , wherein the addition-fragmentation chain transfer functionality is a trithiocarbonate.
23. The mixture of claim 17 , wherein the addition-fragmentation chain transfer functionality is a thiuram disulfide.
24. The mixture of claim 17 , wherein the two polymerizable groups are selected from the group consisting of acrylates, methacrylates, oxiranes (epoxies), amines, vinyl ethers, vinylics, allyl ethers, allylics, thiols, styrenics, isocyanates, and hydroxides, and combinations thereof.
25. The mixture of claim 24 , wherein the two polymerizable groups are each independently selected from the group consisting of acrylates, methacrylates, vinyl ethers and allyl ethers.
26. The mixture of claim 17 , wherein the second monomer is selected from the group consisting of ethylene oxides, ethylene glycols, vinyl acetates, vinyl pyrrolidones, ethyloxazolines, amino acids, saccharides, proteins, anhydrides, vinyl ethers, thiols, amides, carbonates, phenylene oxides, acetals, sulfones, phenylene sulfides, esters, fluoropolymers, imides, amide-imides, etherimides, ionomers, aryletherketones, olefins, styrenes, vinyl chlorides, ethylenes, acrylates, methacrylates, amines, phenols, acids, nitriles, acrylamides, maleates, benzenes, epoxies, cinnamates, azoles, silanes, chlorides, epoxides, lactones, isocyanates, hydroxides and amides.
27. The mixture of claim 26 , wherein the second monomer is an acrylate or a methacrylate.
28. The mixture of claim 17 , further comprising a third ring opening monomer containing an addition-fragmentation chain transfer functionality in the backbone.
29. The mixture of claim 17 wherein a source of free radicals is provided in c), the source of free radicals being a photoinitiator, a thermal initiator, or a redox initiator.
30. The mixture of claim 17 , wherein the mixture further comprises a second source of radicals or cations different from the first.
31. The mixture of claim 17 , wherein the polymeric material is a coating material, a dental material, an optical material, or part of a fiber reinforced composite material.
32. The mixture of claim 4 wherein the polymerizable groups of each of A 1 and A 2 are each independently selected from the group consisting of acrylates, methacrylates, vinyl ethers, allyl ethers, isocyanates and epoxies.
33. The mixture of claim 32 , wherein the second monomer is a thiol.
34. The mixture of claim 5 , wherein the RAFT agent comprises the group
and the polymerizable groups of each of A 1 and A 2 are each independently selected from the group consisting of acrylates, methacrylates, vinyl ethers and allyl ethers.
35. The mixture of claim 34 , wherein the second monomer is an acrylate or methacrylate.