Dual-cure resins and related methods
US-10316213-B1 · Jun 11, 2019 · US
US11518089B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11518089-B2 |
| Application number | US-202017606157-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 21, 2020 |
| Priority date | Apr 30, 2019 |
| Publication date | Dec 6, 2022 |
| Grant date | Dec 6, 2022 |
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Provided herein according to some embodiments is a dual cure additive manufacturing resin, comprising: (i) a light polymerizable component, (ii) a photoinitiator, (iii) a heat polymerizable component, and (iv) a non-reactive diluent, which resin is useful for the production of three-dimensional objects by additive manufacturing. Methods of using the same are also provided.
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We claim: 1. A dual cure additive manufacturing resin, comprising: (i) a light polymerizable component, said light polymerizable component comprising monomers, prepolymers, or both monomers and prepolymers that can be polymerized by exposure to actinic radiation or light, said monomers, prepolymers, or monomers and prepolymers of said light polymerizable component comprising reactive end groups selected from the group consisting of acrylates, methacrylates, alpha-olefins, N-vinyls, acrylamides, methacrylamides, styrenics, epoxides, thiols, 1,3-dienes, vinyl halides, acrylonitriles, vinyl esters, maleimides, and vinyl ethers, (ii) a photoinitiator, (iii) a heat polymerizable component, wherein said heat polymerizable component comprises the precursors to a polyurethane, polyurea, a copolymer of a polyurethane and polyurea, a silicone resin, an epoxy resin, a cyanate ester resin, a copolymer of an epoxy and a cyanate ester resin, or a natural rubber, and (iv) a non-reactive diluent, wherein said non-reactive diluent has a boiling point of from 80 degrees Centigrade to 250 degrees Centigrade and is included in said resin in an amount of from 1 percent by weight to 20 percent by weight. 2. The resin of claim 1 , wherein said non-reactive diluent has a boiling point of from 100 degrees Centigrade to 250 degrees Centigrade. 3. The resin of claim 1 , wherein said resin has a viscosity of not more than 3500 centipoise at 40 degrees Centigrade. 4. The resin of claim 1 , wherein said non-reactive diluent is included in said resin in an amount of from 5 percent by weight to 15 percent by weight. 5. The resin of claim 1 , wherein said non-reactive diluent comprises a glycol ether. 6. The resin of claim 1 , wherein said non-reactive diluent comprises an ester. 7. The resin of claim 1 , wherein said non-reactive diluent comprises an alcohol. 8. The resin of claim 1 , wherein said non-reactive diluent comprises N-methyl-2-pyrrolidone, N,N-dimethylformamide, heavy naptha, toluene, xylene, mineral spirits or white spirits, or a combination of two or more thereof. 9. The resin of claim 1 , wherein said non-reactive diluent comprises dipropylene glycol dimethyl ether, dipropylene glycol methyl ether acetate, or a combination thereof. 10. The resin of claim 1 , wherein said non-reactive diluent has: (i) a boiling point less than 240 degrees Centigrade at a pressure of one bar; and/or (ii) an autoignition temperature less than 600 degrees Centigrade; and/or (iii) a flash point less than 140 degrees Centigrade as measured by the Pensky-Martens closed cup method. 11. The resin of claim 1 , wherein said monomers, prepolymers, or monomers and prepolymers of said light polymerizable component comprise reactive end groups selected from the group consisting of acrylates and methacrylates. 12. The resin of claim 1 , wherein said heat polymerizable component comprises the precursors to a polyurethane, polyurea, or a copolymer of a polyurethane and polyurea. 13. The resin of claim 1 , wherein said light polymerizable component comprises a reactive blocked monomer, a reactive blocked prepolymer, or a combination thereof. 14. The resin of claim 1 , wherein said light polymerizable component comprises a polyisocyanate prepolymer blocked by reaction of a polyisocyanate oligomer with an amine (meth)acrylate, alcohol (meth)acrylate, maleimide, or n-vinylformamide monomer blocking agent. 15. The resin of claim 1 , wherein said heat polymerizable component comprises a polyol and/or polyamine in liquid or solid form. 16. The resin of claim 1 , wherein said resin further comprises at least one, any combination, or all, of: (v) a chain extender; (vi) a reactive diluent; (vii) a pigment or dye; and (viii) a filler. 17. The resin of claim 1 , wherein said resin further comprises an antioxidant. 18. The resin of claim 1 , wherein said resin further comprises a plasticizer. 19. A method of making a three-dimensional (3D) object from a light polymerizable resin, comprising the steps of: (a) providing the dual cure resin of claim 1 ; (b) producing an intermediate 3D object from said resin by light polymerizing said resin in an additive manufacturing process; (c) optionally cleaning said intermediate 3D object; and then (d) heating said intermediate 3D object to volatilize said diluent, polymerize said heat polymerizable component, and produce said three-dimensional object. 20. The method of claim 19 , wherein said producing step is carried out by bottom-up stereolithography. 21. The method of claim 19 , wherein said cleaning step is included. 22. The method of claim 19 , wherein said three-dimensional object produced in step (d) has: (i) a shore A hardness of at least 60; (ii) a Young's modulus of at least 15 MPa, (iii) a percent elongation at break of at least 200, (iv) an ultimate tensile strength of at least 16 MPa, or (v) any combination of the foregoing. 23. The method of claim 19 , wherein said heating step is carried out with said intermediate 3D object in an inert atmosphere. 24. The method of claim 23 , further comprising: (e) concurrently with said heating step, condensing volatilized diluent out of said inert atmosphere in an amount sufficient to reduce the duration of said heating step. 25. A dual cure additive manufacturing resin, comprising: (i) a light polymerizable component, said light polymerizable component comprising monomers, prepolymers, or both monomers and prepolymers that can be polymerized by exposure to actinic radiation or light, said monomers, prepolymers, or monomers and prepolymers of said light polymerizable component comprising reactive end groups selected from the group consisting of acrylates and methacrylates, (ii) a photoinitiator, (iii) a heat polymerizable component, wherein said heat polymerizable component comprises the precursors to a polyurethane, polyurea, or a copolymer of a polyurethane and polyurea, and (iv) a non-reactive diluent, wherein said non-reactive diluent is a glycol ether and has a boiling point of from 80 degrees Centigrade to 250 degrees Centigrade and is included in said resin in an amount of from 1 percent by weight to 20 percent by weight. 26. The resin of claim 25 , wherein said non-reactive diluent comprises dipropylene glycol dimethyl ether, dipropylene glycol methyl ether acetate, or a combination thereof. 27. The resin of claim 25 , wherein said light polymerizable component comprises a reactive blocked monomer, a reactive blocked prepolymer, or a combination thereof. 28. The resin of claim 25 , wherein said light polymerizable component comprises a polyisocyanate prepolymer blocked by reaction of a polyisocyanate oligomer with an amine (meth)acrylate, alcohol (meth)acrylate, maleimide, or n-vinylformamide monomer blocking agent. 29. The resin of claim 25 , wherein said heat polymerizable component comprises a polyol and/or polyamine in liquid or solid form.
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