Method for fabrication of additively manufactured, self-gelling structures and their use
US-2024245836-A1 · Jul 25, 2024 · US
US2016279870A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016279870-A1 |
| Application number | US-201615172347-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 3, 2016 |
| Priority date | Mar 9, 2011 |
| Publication date | Sep 29, 2016 |
| Grant date | — |
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In one aspect, build materials operable for use in 3D printing systems are described herein. In some embodiments, a build material comprises an oligomeric curable material, a reactive component that is solid at 25° C., and at least one diluent, wherein the reactive component comprises at least one chemical moiety that is polymerizable with a chemical moiety contained in the oligomeric curable material and/or the at least one diluent.
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That which is claimed: 1 . A method of printing a three dimensional article comprising: selectively depositing layers of a fluid build material to form the three dimensional article on a substrate, wherein the build material comprises: an oligomeric curable material; a reactive component; a non-reactive component comprising one or more urethane waxes; and at least one diluent, wherein the reactive component comprises at least one chemical moiety that is polymerizable with a chemical moiety contained in the oligomeric curable material and/or the at least one diluent and wherein the reactive component is present in the build material as crystalline regions. 2 . The method of claim 1 , wherein the layers of the build material are deposited according to an image of the three dimensional article in a computer readable format. 3 . The method of claim 1 further comprising supporting at least one of the layers of the build material with a support material. 4 . The method of claim 1 further comprising curing the build material. 5 . The method of claim 1 , wherein the build material solidifies upon deposition. 6 . The method of claim 1 , wherein the build material remains substantially fluid upon deposition. 7 . The method of claim 1 , wherein the non-reactive component does not comprise a chemical moiety that is polymerizable with a chemical moiety contained in the oligomeric curable material or the at least one diluent. 8 . The method of claim 1 , wherein the build material further comprises one or more additives selected from the group consisting of photoinitiators, inhibitors, stabilizing agents, sensitizers, and combinations thereof. 9 . The method of claim 1 , wherein the oligomeric curable material is a urethane (meth)acrylate having a viscosity ranging from 10,000 cps to 300,000 cps. 10 . The method of claim 1 , wherein the oligomeric curable material and the reactive component each contain one or more acrylate or (meth)acrylate moieties. 11 . The method of claim 1 , wherein the reactive component comprises more than one chemical moiety that is polymerizable with a chemical moiety contained in the oligomeric curable material and/or the at least one diluent. 12 . The method of claim 1 , wherein the reactive component comprises at least one of the following: a urethane (meth)acrylate, a urea (meth)acrylate, and an isocyanurate (meth)acrylate. 13 . The method of claim 1 , wherein the reactive component is selected from the group consisting of: (i) an isocyanurate tri(meth)acrylate; (ii) a species defined by the formula R 1 —NHCOO—R 2 —R 3 , wherein R 1 is C n H (2n+2) (wherein n=4-36), R 2 is C n H (2n+2) (wherein n=2-36), and R 3 is —OCOCH═CH 2 or —OCOC(CH 3 )═CH 2 ; (iii) a species defined by the formula R 1 —R 2 —NHCOO—R 3 —OOC—NH—R 2 —R 1 , wherein R 1 is —OCOCH═CH 2 or —OCOC(CH 3 )═CH 2 , R 2 is C n H (2n+2) (wherein n=2-36), and R 3 is C n H (2n+2) (wherein n=2-36); (iv) a species defined by the formula R 1 —NHCONH—R 2 —R 3 , wherein R 1 is C n H (2n+2) (wherein n=4-36), R 2 is C n H (2n+2) (wherein n=2-36), and R 3 is —OCOCH═CH 2 or —OCOC(CH 3 )═CH 2 ; and (v) a species defined by the formula R 1 —R 2 —NHCONH—R 3 —OOC—NH—R 2 —R 1 , wherein R 1 is —OCOCH═CH 2 or —OCOC(CH 3 )═CH 2 , R 2 is C n H (2n+2) (wherein n=2-36), and R 3 is C n H (2n+2) (wherein n=2-36). 14 . The method of claim 1 , wherein the reactive component comprises a nitrogen-containing ring. 15 . The method of claim 1 , wherein the reactive component is an isocyanurate. 16 . The method of claim 1 , wherein the reactive component is tris(2-hydroxy ethyl)isocyanurate triacrylate. 17 . The method of claim 1 , wherein the reactive component comprises 5 to 50 percent by weight of the build material. 18 . The method of claim 1 , wherein the reactive component comprises 5 to 15 percent by weight of the build material. 19 . The method of claim 1 , wherein the reactive component exhibits a melting point range of 1° C. to 10° C., centered between 40° C. and 100° C. 20 . The method of claim 1 , wherein the at least one diluent contains one or more (meth)acrylate moieties.
with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen · CPC title
having terminal carbon-to-carbon unsaturated bonds · CPC title
Processes of additive manufacturing · CPC title
Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] · CPC title
for controlling or regulating additive manufacturing processes · CPC title
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