Non-hazardous water-based polyurethane dispersion
US-12110373-B2 · Oct 8, 2024 · US
US9822279B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9822279-B2 |
| Application number | US-201214235582-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 24, 2012 |
| Priority date | Aug 26, 2011 |
| Publication date | Nov 21, 2017 |
| Grant date | Nov 21, 2017 |
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The invention relates to a two-component composition, including a component A, which includes at least one silane-functional polymer and at least one hardener or accelerator for epoxy resins, and a component B, which includes at least one aqueous emulsion of at least one epoxy resin. Two-component compositions according to the invention are suitable as adhesives, sealants or coatings.
Opening claim text (preview).
The invention claimed is: 1. A method of adhesive bonding, sealing, or coating a substrate, comprising: mixing a component A and a component B of a two-component composition together to obtain a hardenable composition; applying the hardenable composition to the substrate; and hardening the hardenable composition applied to the substrate, wherein: component A, at the time of mixing, comprises at least one silane-functional polymer, and at least one hardener or accelerator for epoxy resins; component B, at the time of mixing, comprises at least one aqueous emulsion including epoxy resin particles and an emulsifier formed by emulsifying at least one liquid epoxy resin in the presence of the emulsifier and water; the silane-functional polymer includes (i) a silane-functional polyurethane polymer obtainable by reacting a silane that includes at least one group reactive toward isocyanate groups and a polyurethane polymer that includes isocyanate groups, or (ii) a silane-functional polyurethane polymer obtainable by reacting an isocyanatosilane and a polymer that includes functional end groups reactive toward isocyanate groups; and the epoxy resin particles have a mean particle size in the range of 0.05 to 10 μm. 2. The method according to claim 1 , wherein the aqueous emulsion contains 10 to 40% by weight of water. 3. The method according to claim 1 , wherein the emulsion has a particle size distribution, in which the size ratio of the largest to the smallest particles has a value in the range of ≦25. 4. The method according to claim 1 , wherein 90% of the particles in the emulsion are smaller than 6 μm. 5. The method according to claim 1 , wherein the hardener or accelerator for epoxy resins is selected from the group consisting of tertiary polyamines, Mannich bases, polymercaptans and imidazoles. 6. The method according to claim 1 , wherein the hardener or accelerator for epoxy resins is selected from the group consisting of pentamethyl-diethylenetriamine, N,N-dimethyl-N′-(dimethylamino-propyl)-1,3-propanediamine, bis(2-dimethylaminoethyl)ether, bis-(-dimethyl-aminoethyl)-piperazine, N,N′-dimethylpiperazine, dimethylaminomethyl-phenol, 2,4,6-tris(dimethyl-aminomethyl)-phenol, 2,4,6-tris((3-(dimethylamino)propyl)-aminomethyl)phenol, 1-methylimidazole, 1-ethylimidazole, 1-vinylimidazole, 2-methylimidazole, 2-ethylimidazole, 2-isopropylimidazole, 2-heptadecylimidazole, 2-ethyl-4-methylimidazole and 1-benzyl-2-methylimidazole. 7. The method according to claim 1 , wherein the two-component composition further comprises at least one catalyst for cross-linking the silane-functional polymer with the aid of moisture. 8. The method according to claim 7 , wherein the catalyst for cross-linking the silane-functional polymer using moisture is selected from the group consisting of organotin compounds, titanates, zirconates, tertiary amines, amidines and guanidines. 9. The method according to claim 1 , wherein the two-component composition further comprises at least one aminosilane, an epoxysilane or a mercaptosilane. 10. The method according to claim 1 , wherein the two-component composition further comprises at least one filler. 11. The method according to claim 1 , wherein the fraction of the hardener or accelerator for epoxy resins is 0.5 to 15% by weight based on component A. 12. The method according to claim 1 , wherein the weight ratio of component A to component B is 1:1 to 100:1. 13. The method according to claim 1 , wherein hardening the hardenable composition results in a partially hardened composition. 14. The method according to claim 1 , wherein hardening the hardenable composition results in a completely hardened composition. 15. The method according to claim 1 , wherein the silane-functional polymer is the polymer of (i), in which the silane is a mercaptosilane or an aminosilane. 16. The method according to claim 1 , wherein the weight ratio of component A to component B is 2.5:1 to 100:1. 17. The method according to claim 1 , wherein component A is in a non-aqueous system at the time of coming into contact with component B. 18. The method according to claim 1 , wherein the aqueous emulsion has a solids content of 70 to 90% by weight. 19. A method of adhesive bonding, sealing, or coating a substrate, comprising: mixing a component A and a component B of a two-component composition together to obtain a hardenable composition; applying the hardenable composition to the substrate; and hardening the hardenable composition applied to the substrate, wherein: component A, at the time of mixing, comprises at least one silane-functional polymer, and at least one hardener or accelerator for epoxy resins; component B, at the time of mixing, comprises at least one aqueous emulsion including epoxy resin particles and an emulsifier formed by emulsifying at least one liquid epoxy resin in the presence of the emulsifier and water; component A is in a non-aqueous system prior to coming into contact with component B; and the epoxy resin particles have a mean particle size in the range of 0.05 to 10 μm. 20. The method according to claim 19 , wherein the silane-functional polymer includes (i) a silane-functional polyurethane polymer obtainable by reacting a silane that includes at least one group reactive toward isocyanate groups and a polyurethane polymer that includes isocyanate groups, (ii) a silane-functional polyurethane polymer obtainable by reacting an isocyanatosilane and a polymer that includes functional end groups reactive toward isocyanate groups, or (iii) a silane-functional polymer obtainable by a hydroxysilylation reaction of polymers with terminal double bonds. 21. The method according to claim 19 , wherein the aqueous emulsion has a solids content of 70 to 90% by weight.
by silicon containing compounds · CPC title
Compositions of epoxy resins; Compositions of derivatives of epoxy resins · CPC title
from compounds containing nitrogen and active hydrogen, the nitrogen atom not being part of an isocyanate group · CPC title
containing hydrolysable silane groups · CPC title
containing silicon · CPC title
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