Electrical steel sheet and method for manufacturing same
US-12163066-B2 · Dec 10, 2024 · US
US10501592B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10501592-B2 |
| Application number | US-201815859991-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 2, 2018 |
| Priority date | Jun 30, 2015 |
| Publication date | Dec 10, 2019 |
| Grant date | Dec 10, 2019 |
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The present invention relates to a process for cold bonding elastomeric rubber substrates to non-elastomeric substrates of a different material, preferably metal, by use of a rubber treatment, preferably a primer composition and a 2k adhesive, preferably a 2k epoxy adhesive as well as the thus obtained bonded substrates.
Opening claim text (preview).
What is claimed: 1. A process for forming a bond between a first elastomeric rubber substrate and a second metal substrate, comprising: providing the elastomeric rubber substrate; providing the metal substrate; applying an oxidizing rubber treatment and/or a primer composition comprising at least one cyanoacrylate to a to-be-bonded surface of the rubber substrate; providing a curable 2K adhesive comprising a resin component and a hardener component; mixing the resin component and hardener component to form a mixed 2K adhesive composition; applying the mixed 2K adhesive composition to a to-be-bonded surface of the metal substrate; incubating the applied 2K adhesive composition for 0.5 to 10 hours to develop green strength; and contacting the primed surface of the rubber substrate and the applied adhesive on the surface of the metal substrate to form the bond. 2. The process according to claim 1 , wherein the 2K adhesive is selected from the group consisting of a 2k polyurea adhesive and a 2k epoxy adhesive. 3. The process according to claim 1 , wherein the oxidizing rubber treatment comprises an oxidizing compound selected from the group consisting of iodine monobromide and sodium hypochlorite. 4. The process according to claim 1 , wherein the cyanoacrylate is a 2-cyanoacrylate ester of Formula (I) H 2 C═C(CN)—COOR (I), wherein R is selected from the group consisting of C 1-20 alkyl optionally substituted with halogen, C 2-16 alkenyl or alkynyl group, C 5-8 cycloalkyl, C 6-14 aryl, alkylaryl, alkoxyalkyl, and acylalkyl, preferably C 1-4 alkyl, more preferably ethyl or methyl. 5. The process according to claim 1 , wherein the cyanoacrylate is a 2-cyanoacrylate ester of Formula (I) H 2 C═C(CN)—COOR (I), wherein R is ethyl or methyl. 6. The process according to claim 1 , wherein the cyanoacrylate is ethyl cyanoacrylate. 7. The process according to claim 1 , wherein the oxidizing rubber treatment and/or the primer composition further comprises up to 40 wt.-% of an organic solvent relative to the oxidizing rubber treatment or primer composition respectively. 8. The process according to claim 1 , wherein: the 2k adhesive is a 2k epoxy adhesive; the resin component comprises a liquid bisphenol A-based epoxy resin, optionally modified with phenoxy and/or a liquid bisphenol F-based epoxy resin, optionally modified with phenoxy; and/or the hardener component comprises at least one difunctional mercaptan and/or at least one mercaptane-epoxy adduct and/or at least one member selected from the group consisting of polyamines, polyamides, low molecular weight amines. 9. The process according to claim 1 , wherein the 2k adhesive is a 2k polyurea adhesive wherein the hardener component comprises 1) at least one oligomeric amine, and/or 2) at least one amine selected from the group consisting of polyamines, low molecular weight amines and combinations thereof, and the resin component comprises 3) at least one isocyanate containing material including at least one aliphatic isocyanate, at least one aromatic isocyanate, or isocyanate functional prepolymers of the aliphatic isocyanate or aromatic isocyanate. 10. The process according to claim 1 , carried out at a temperature of 15-40° C. and a relative humidity below 85%. 11. The process according to claim 1 , wherein the curable 2K adhesive comprises a curing indicator to indicate when the applied adhesive has developed sufficient green strength to contact the primed surface of the rubber substrate to the applied adhesive on the surface of the metal substrate. 12. The process according to claim 1 , wherein the adhesive composition comprises a color changing azo dye. 13. The process according to claim 1 , further comprising a step of cleaning the to-be-bonded surface of the rubber substrate prior to applying the oxidizing rubber treatment and/or a step of cleaning to-be-bonded surface of the metal substrate prior to applying the mixed 2K adhesive composition. 14. The process according to claim 1 , wherein the primer composition is applied in an amount of 70-190 g/m 2 or in an amount of 300-500 g/m 2 . 15. The process according to claim 1 , further comprising a step of drying the oxidizing rubber treatment and/or a primer composition applied to the to-be-bonded surface before the step of contacting. 16. The process according to claim 1 , wherein the step of incubating comprises incubating the mixed 2K adhesive composition for 0.5 to 10 hours at ambient temperature until the mixed adhesive has a floating roller peel resistance of 0.5 N/mm to 3 N/mm (ASTMD3167-03). 17. The process according to claim 1 , wherein the step of contacting the primed surface of the rubber substrate and the applied adhesive on the surface of the metal substrate is carried out by rolling. 18. The process according to claim 1 , wherein the step of incubating comprises incubating the mixed 2K adhesive composition for 0.5 to 10 hours at ambient temperature until the mixed adhesive has a viscosity of 250 to 15,000 Pas.
in the primer coating · CPC title
in the pretreated surface to be joined · CPC title
organic · CPC title
Adhesives based on epoxy resins; Adhesives based on derivatives of epoxy resins · CPC title
in the release coating · CPC title
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