Radiation curable resin compositions are provided that are most useful in stereolithography. A radiation curable resin includes a base oligomer, a cross linking agent, a reactive solvent, and an anti-nucleation agent. The resin after curing provides a solid product that has improved physical propert
Radiation curable resin compositions are provided that are most useful in stereolithography. A radiation curable resin includes a base oligomer, a cross linking agent, a reactive solvent, and an anti-nucleation agent. The resin after curing provides a solid product that has improved physical properties.
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What is claimed is: 1. A liquid stereolithography resin comprising a base oligomer, a reactive solvent, a cross linking agent, and an anti-nucleation agent or a pnictide-containing compound. 2. The liquid stereolithography resin of claim 1, wherein the anti-nucleation agent is a flame-retardant
What is claimed is: 1. A liquid stereolithography resin comprising a base oligomer, a reactive solvent, a cross linking agent, and an anti-nucleation agent or a pnictide-containing compound. 2. The liquid stereolithography resin of claim 1, wherein the anti-nucleation agent is a flame-retardant additive. 3. The liquid stereolithography resin of claim 1, further comprising a photoinitiator. 4. The liquid stereolithography resin of claim 3, wherein the photoinitiator includes a phosphine oxide, an alpha-hydroxyketone, and a benzophenone derivative. 5. The liquid stereolithography resin of claim 3, wherein the photoinitiator includes a component selected from the group consisting of a 2-hydroxy-2-methyl-1-phenyl-1-propanone, a 2,4,6-trimethylbenzoyl-diphenyl-phosphineoxide, or a combination thereof. 6. The liquid stereolithography resin of claim 3, wherein the photoinitiator includes a component selected from the group consisting of a blend of 2,4,6-trimethylbenzoyl-diphenyl-phosphineoxide and hydroxy-2-methyl-1-phenyl-propan-1-one, a phosphine oxide, a 2-hydroxy-2-methyl-1-phenyl-1-propanone, and mixtures thereof. 7. The liquid stereolithography resin of claim 3, wherein the photoinitiator activates polymerization of an acrylate in a wavelength range of 240 nm to 250 nm, 360 nm to 380 nm, or 390 nm to 410 nm. 8. The liquid stereolithography resin of claim 1, wherein the base oligomer includes an aliphatic urethane diacrylate. 9. The liquid stereolithography resin of claim 8, wherein the aliphatic urethane diacrylate is an aliphatic polyester urethane diacrylate. 10. The liquid stereolithography resin of claim 1, wherein the reactive solvent includes a monovalent acrylate. 11. The liquid stereolithography resin of claim 1, wherein the reactive solvent includes a polyvalent acrylate. 12. The liquid stereolithography resin of claim 1, wherein the base oligomer has formula (I): wherein each M1 is, independently, an alkylene, an acylalkylene, an oxyalkylene, an arylene, an acylarylene, or an oxyarylene, M1 being optionally substituted with alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, acyl, alkoxy, hydroxyl, hydroxylalkyl, halo, haloalkyl, amino, silicone, aryl, or aralkyl, each M2 is, independently, an alkylene or an arylene, M2 being optionally substituted with alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, acyl, alkoxy, hydroxyl, hydroxylalkyl, halo, haloalkyl, amino, silicone, aryl, or aralkyl, each A, independently, has the formula: wherein R1 is hydrogen or lower alkyl, each L is, independently, C1-C4 alkyl, and w is an integer ranging from 0 to 20, and x is a positive integer less than 40, y is a positive integer less than 100, z is a positive integer less than 40, and w, x, y, and z together are selected such that the molecular weight of the base oligomer is less than 20,000. 13. The liquid stereolithography resin of claim 12, wherein M1 is a straight, branched, or cyclic alkylene. 14. The liquid stereolithography resin of claim 12, wherein M1 is an acylalkylene or acylarylene. 15. The liquid stereolithography resin of claim 14, wherein M2 is a straight, branched, or cyclic alkylene. 16. The liquid stereolithography resin of claim 12, wherein M2 is a straight, branched, or cyclic alkylene. 17. The liquid stereolithography resin of claim 12, wherein L is branched or unbranched C1-C4 alkyl. 18. The liquid stereolithography resin of claim 12, wherein the reactive solvent has formula (II): description="In-line Formulae" end="lead"A'-O--R2--(O-A') (II) description="In-line Formulae" end="tail" wherein R2 is a monovalent or polyvalent moiety selected from the group consisting of a C1-C12 aliphatic group, an aromatic group, and a poly(C1-C4 branched or unbranched alkyl ether), R2 being optionally substituted with alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, acyl, alkoxy, hydroxyl, hydroxylalkyl, halo, haloalkyl, amino, aryl, or aralkyl, n is an integer ranging from 0 to 5, and each A' has the formula: wherein R1 is hydrogen or lower alkyl, each L independently is C1-C4 alkyl, and w is an integer ranging from 0 to 20. 19. The liquid stereolithography resin of claim 1, wherein the reactive solvent has formula (II): description="In-line Formulae" end="lead"A'-O--R2--(O-A') (II) description="In-line Formulae" end="tail" wherein R2 is a monovalent or polyvalent moiety selected from the group consisting of a C1-C12 aliphatic group, an aromatic group, and a poly(C1-C4 branched or unbranched alkyl ether), R2 being optionally substituted with alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, acyl, alkoxy, hydroxyl, hydroxylalkyl, halo, haloalkyl, amino, aryl, or aralkyl, n is an integer ranging from 0 to 5, and each A' has the formula: wherein R1 is hydrogen or lower alkyl, each L independently is C1-C4 alkyl, and w is an integer ranging from 0 to 20. 20. The liquid stereolithography resin of claim 19, wherein L is branched or unbranched C1-C4 alkyl. 21. The liquid stereolithography resin of claim 1, wherein the reactive solvent agent includes an acrylate monomer. 22. The liquid stereolithography resin of claim 21, wherein the reactive solvent has formula (III): wherein j is 1, 2, 3 or 4, k is equal to 4-j, R3 is hydrogen or C1-C4 branched or unbranched alkyl, each L' independently is C1-C4 branched or unbranched alkyl, each i independently is 0, 1, 2 or 3, and each A" independently has the formula: wherein R1 is hydrogen or lower alkyl, each L independently is C1-C4 branched or unbranched alkyl, and w is an integer ranging from 0 to 20. 23. The liquid stereolithography resin of claim 1, wherein the cross linking agent includes a urethane acrylate oligomer. 24. The liquid stereolithography resin of claim 1, wherein the cross linking agent is a tris(2-hydroxyethyl)isocyanurate triacrylate or ethoxylated (4) bisphenol dimethyacrylate, or a mixture thereof. 25. The liquid stereolithography resin of claim 1, wherein the reactive solvent includes isobornyl acrylate, isobornyl methacrylate, and combinations thereof. 26. The liquid stereolithography resin of claim 1, further comprising a stabilizer. 27. The liquid stereolithography resin of claim 26, wherein the stabilizer is selected from the group consisting of Tinuvin 292 (bis(1,2,2,6,6-pentamethyl-4-piperidyl)sebacate and 1-methyl-10-(1,2,2,6,6-pentamethyl-4-piperidyl)sebacate), Tinuvin 765 (bis(1,2,2,6,6-pentamethyl-4-piperidyl)sebacate), MEQH (4-methoxyphenol), 2-(2'-hydroxy-5'-methylphenyl)benztriazole, 1,2,2,6,6-pentamethyl-4-piperidyl methacrylate and Chimassorb 81 (2-hydroxy-4-octyloxybenzophenone). 28. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN964, the reactive solvent is ethoxylated (3) trimethylolpropane acrylate, and the cross linking agent is selected from the group consisting of isobornyl acrylate, ethoxylated (5) pentaerythritol tetraacrylate, CN965, tris-(2-hydroxyethyl)isocyanurate triacrylate, and mixtures thereof. 29. The liquid stereolithography resin of claim 28, wherein the resin includes 5-35 weight % CN964 and 0.5-25 weight % ethoxylated (3) trimethylolpropane acrylate. 30. The liquid stereolithography resin of claim 29, wherein the resin includes 0.5-20 weight % isobornyl acrylate. 31. The liquid stereolithography resin of claim 29, wherein the resin includes 15-45 weight % ethoxylated (5) pentaerythritol tetraacrylate. 32. The liquid stereolithography resin of claim 29, wherein the resin includes 0.5-25 weight % CN965. 33. The liquid stereolithography resin of claim 29, wherein the resin includes 5-35 weight % tris-(2-hydroxyethyl)isocyanurate triacrylate. 34. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN963, the reactive solvent is tripropyleneglycol diacrylate, and the cross linking agent is selected from the group of CN970H75, ethoxylated (4) bisphenol A dimethyacrylate, isobornyl acrylate, and mixtures thereof. 35. The liquid stereolithography resin of claim 34, wherein the resin includes 40-70 weight % CN963, and 5-35 weight % tripropyleneglycol diacrylate. 36. The liquid stereolithography resin of claim 35, wherein the resin includes 0.5-15 weight % CN970H75. 37. The liquid stereolithography resin of claim 35, wherein the resin includes 0.5-15 weight % ethoxylated (4) bisphenol A dimethyacrylate. 38. The liquid stereolithography resin of claim 35, wherein the resin includes 5-35 weight % isobornyl acrylate. 39. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN966, the reactive solvent is isobornyl acrylate, and the cross linking agent is selected from the group consisting of isobornyl acrylate, ethoxylated (4) bisphenol A dimethyacrylate, and mixtures thereof. 40. The liquid stereolithography resin of claim 39, wherein the resin includes 10-40 weight % CN966 and 0.5-25 weight % isobornyl acrylate. 41. The liquid stereolithography resin of claim 39, wherein the resin includes 6-35 weight % isobornyl acrylate. 42. The liquid stereolithography resin of claim 39, wherein the resin includes 25-55 weight % ethoxylated (4) bisphenol A dimethyacrylate. 43. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN990, the reactive solvent is isobornyl acrylate, and the cross linking agent is selected from the group consisting of CN131, a polyether modified acryl functional polydimethylsiloxane, and mixtures thereof. 44. The liquid stereolithography resin of claim 43, wherein the resin includes 50-80 weight % CN990 and 0.5-20 weight % isobornyl acrylate. 45. The liquid stereolithography resin of claim 44, wherein the resin includes 5-35 weight % CN131. 46. The liquid stereolithography resin of claim 44, wherein the resin includes 0.5-15 weight % A polyether modified acryl functional polydimethylsiloxane. 47. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN973, the reactive solvent is isobornyl acrylate, and the cross linking agent is isobornyl acrylate. 48. The liquid stereolithography resin of claim 47, wherein the resin includes 45-75 weight % CN973 and 10-70 weight % isobornyl acrylate. 49. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN963, the reactive solvent is tripropyleneglycol diacrylate, and the cross linking agent is selected from the group consisting of CN2400, isobornyl acrylate, and mixtures thereof. 50. The liquid stereolithography resin of claim 49, wherein the resin includes 20-50 weight % CN963 and 0.5-25 weight % tripropyleneglycol diacrylate. 51. The liquid stereolithography resin of claim 50, wherein the resin includes 10-40 weight % CN2400. 52. The liquid stereolithography resin of claim 50, wherein the resin includes 10-40 weight % isobornyl acrylate. 53. The liquid stereolithography resin of claim 1, wherein the base oligomer is CN966, the reactive solvent is isobornyl acrylate, and the cross linking agent is selected from the group consisting of CN131 and isobornyl acrylate. 54. The liquid stereolithography resin of claim 53, wherein the resin includes 35-60 weight % CN966 and 10-25 weight % isobornyl acrylate. 55. The liquid stereolithography resin of claim 53, wherein the resin includes 10-45 weight % isobornyl acrylate. 56. The liquid stereolithography resin of claim 53, wherein the resin includes 5-35 weight % CN131. 57. The liquid stereolithography resin of claim 1, wherein the pnictide-containing compound is an organopnictide. 58. The liquid stereolithography resin of claim 1, wherein the pnictide-containing compound is a halogenated organopnictide. 59. A method of forming a three-dimensional object comprising: heating a base oligomer; heating a cross linking agent; mixing the oligomer and cross linking agent together to form a mixture; adding reactive solvent to form a resin; adding an anti-nucleation agent or a pnictide-containing compound to the resin; and selectively exposing the resin to light to form a solidified layer. 60. The method of claim 59, further comprising adding a photoinitiator or a stabilizer. 61. The method of claim 59, wherein the desired characteristic of the finished product is dimensional stability and the precursor is isobornyl acrylate. 62. A method of forming a three-dimensional object comprising: selectively exposing to actinic radiation a first portion of a resin including a base oligomer, a reactive solvent, a cross linking agent, and an anti-nucleation agent or a pnictide-containing compound to form a first solidified layer; and selectively exposing to actinic radiation a second portion of the resin to form a second solidified layer adjacent to the first solidified layer. 63. A method of forming a three-dimensional object comprising: heating a base oligomer; heating a cross linking agent; mixing the oligomer and cross linking agent together to form a mixture; adding reactive solvent to form a resin; adding a pnictide-containing compound to the resin; and selectively exposing the resin to light to form a solidified layer.
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