Three-Dimensional Printing Using Carriers with Release Mechanisms
US-2017210077-A1 · Jul 27, 2017 · US
US10239238B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10239238-B2 |
| Application number | US-201715486128-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 12, 2017 |
| Priority date | Apr 15, 2016 |
| Publication date | Mar 26, 2019 |
| Grant date | Mar 26, 2019 |
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The present disclosure concerns a digital fabricating method for constructing 3D structures, comprising the following steps: (a) precursor consist of monomers and photo-initiator is introduced into reaction cell; (b) exposing the precursor to the DLP projector for several times to gain an inhomogeneous sheet; (c) swelling the sheet in solvent to gain 3D structure. The disclosure provides a simple and easy way to produce precise 3D structure.
Opening claim text (preview).
The invention claimed is: 1. A method for constructing 3D polymer structures with digital light patterning technology, comprising the following steps: (a) introducing photo-curable precursors comprising monomers and photo-initiators into a flat reaction cell; (b) using a DLP-type projector to illuminate and cure the precursor locally and cumulatively, getting a heterogeneous 2D polymer sheet; (c) swelling the 2D polymer sheet in a certain solvent or heat the sheet until reaching a equilibrium 3D structure. 2. The method of claim 1 , wherein the monomers can be chosen from acrylate monomers and epoxy monomers, the acrylate monomers have at least two acrylate functional groups; the epoxy monomers have at least two epoxy functional groups. 3. The method of claim 2 , wherein the acrylate monomers can be chosen from poly(ethylene glycol) diacrylate, ethylene glycol diacrylate, epoxy acrylate, polyurethane acrylate, polyester acrylate and amino acrylic resin; the epoxy monomers can be chosen from bisphenol A epoxy, bisphenol F epoxy and cycloaliphatic epoxy. 4. The method of claim 3 , wherein the acrylate monomers selectively include a monomer with one acrylate functional group; the epoxy monomers selectively include a monomer with one epoxy functional group as reactive diluent. 5. The method of claim 1 , wherein the radical photo-initiator is chosen for the acrylate monomer, the cationic photo-initiator is chosen for the epoxy monomer, the amount of the photo-initiator ranges from 0.1 to 5% by weight. 6. The method of claim 5 , wherein the radical photo-initiator can be chosen from benzoin, benzoin dimethyl ether, 2-phenylacetophenone, benzoin dimethyl ether, hydroxyalkyl phenyl ketone, aroyl phosphorus oxide, diphenyl ketone, 2,4-Dihydroxybenzophenone, 2-isopropylthioxanthone and cationic photo-initiator can be chosen from diaryliodonium salts, triaryliodonium salts, alkyl iodonium salt, cumene ferrocene hexafluorophosphate. 7. The method of claim 1 , wherein the reaction cell is constructed by piling up two quartz glass sheets separated with silicon spacer and the spacer thickness is in the range of 0.3 mm to 5 mm. 8. The method of claim 1 , wherein the DLP-type projector is connected to a computer through an open source G-code and graphics software. 9. The method of claim 1 , wherein the light source of the projector can be a mercury lamp with all band ultraviolet or a LED lamp with specific wavelength coincidence with the photo-initiator such as 315 nm, 365, 405 nm. 10. The method of claim 1 , wherein the solvent used to swell the 2D polymer sheet is chosen according to the hydrophilicity of the polymer.
Local curing (for repairing B29C73/34) · CPC title
Use of {EP, i.e.} epoxy resins {or derivatives thereof}, as moulding material · CPC title
monomers or prepolymers · CPC title
using liquids, e.g. solvents, swelling agents (spectacle cases, e.g. for cleaning contact lenses A45C11/04; disinfecting or sterilising contact lenses A61L12/00, using liquid substances A61L2/20; cleaning involving the use of liquid in general B08B3/00; for hydrating contact lenses B29D11/00067) · CPC title
using UV radiation · CPC title
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