IP Library Granted Patent US 11,639,031
Granted Patent B2
US 11,639,031 · App. 15/930,822 · Granted May 2, 2023

Photocurable resins for volumetric additive manufacturing

Inventors: Maxim Shusteff (Piedmont, CA); James Oakdale (Castro Valley, CA); Robert Matthew Panas (Dublin, CA); Christopher M. Spadaccini (Oakland, CA); Hayden K. Taylor (Berkeley, CA); Brett Kelly (Berkeley, CA); Indrasen Bhattacharya (Berkeley, CA); Hossein Heidari (Berkeley, CA)
Assignees: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC; THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
B29C64/393B29C64/153B29C64/232B33Y10/00B33Y30/00B33Y50/02C08F2/50C08F20/18B29C64/106B29C64/124B29C64/241B29C64/264B29C64/268B29C64/277B29C64/282B29C64/386B29K2033/08B33Y40/20B33Y70/10
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Quick Facts
Patent No.
US 11,639,031
App. No.
15/930,822
Granted
May 2, 2023
Kind
B2
Abstract

Methods and materials for volumetric additive manufacturing, including computed axial lithography (“CAL”), using photosensitive resins comprising a photocurable resin prepolymer; a photoinitiator; and (optionally) a curing inhibitor. In various embodiments, such photosensitive polymers comprise (a) one or more monomer (or prepolymer) molecules, which form the backbone of the polymer network of the polymeric material and define its architecture; and (b) a photoinitiator that captures illumination energy and initiates polymerization.

Claims (18)

1. A method of forming a three dimensional (3D) object, comprising:

simultaneously directing optical projections of light from optical subsystems at a plurality of angles θ through a volume of photocurable composition contained within an optically transparent resin container, the optical projections further being directed about a z axis extending through the volume of photocurable composition; and

providing each of the optical projections with a calculated three-dimensional intensity distribution acting over a fixed temporal exposure period, which is sufficient to cure selected portions of the volume of photocurable composition, and leave other portions unmodified, to form the 3D object;

wherein the photocurable composition comprises a monomer, a photoinitiator, and a curing inhibitor, and exhibits transparency to the light and a non-linear response to the light.

2. The method of claim 1 , wherein the curing inhibitor is selected from the group consisting of oxygen; (2,2,6,6-Tetramethyl-1-piperidinyloxy); phenothiazine; 4-methoxyphenol; N-Nitroso-N-phenylhydroxylamine aluminum salt; tetraethylthiuram disulfide; Di-tert-butyl nitroxide; 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide; and combinations thereof.

3. The method of claim 2 , wherein the curing inhibitor comprises oxygen and the monomer is an acrylate.

4. The method of claim 1 , wherein the photocurable composition further has a viscosity of at least 1000 cP.

5. The method of claim 1 , wherein a change in refractive index of the photocurable composition upon curing is not greater than 0.01.

6. A method of forming a three dimensional (3D) object, comprising:

simultaneously directing optical projections of light from optical subsystems at a plurality of angles θ through a volume of photocurable composition contained within an optically transparent resin container, the optical projections further being directed about a z axis extending through the volume of photocurable composition; and

providing each of the optical projections with a calculated three-dimensional intensity distribution acting over a fixed temporal exposure period, which is sufficient to cure selected portions of the volume of photocurable composition, and leave other portions unmodified, to form the 3D object;

wherein the photocurable composition comprises a monomer, a photoinitiator, and a curing inhibitor, and exhibits transparency to the light and a non-linear response to the light; and

wherein a change in refractive index of the photocurable composition upon curing is not greater than 0.03.

7. The method of claim 6 , wherein the change in refractive index of the photocurable composition upon curing is not greater than 0.01.

8. The method of claim 6 , wherein the curing inhibitor is selected from the group consisting of oxygen; (2,2,6,6-Tetramethyl-1-piperidinyloxy); phenothiazine; 4-methoxyphenol; N-Nitroso-N-phenylhydroxylamine aluminum salt; tetraethylthiuram disulfide; Di-tert-butyl nitroxide; 2,2,5-Trimethyl-4-phenyl-3-azahexane-3-nitroxide; and combinations thereof.

9. The method of claim 7 , wherein the curing inhibitor comprises oxygen and the monomer is an acrylate.

10. The method of claim 6 , wherein the photocurable composition further has a viscosity of at least 1000 cP.

11. The method of claim 6 , wherein the photoinitiator is a Norrish Type I or Type II photoinitiator.

Assignments (3)
CONFIRMATORY LICENSE (SEE DOCUMENT FOR DETAILS) Recorded Aug 26, 2020
From: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
To: U.S. DEPARTMENT OF ENERGY
Reel/Frame 053603/0548 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2020
From: SHUSTEFF, MAXIM; OAKDALE, JAMES; PANAS, ROBERT MATTHEW; SPADACCINI, CHRISTOPHER M.; KELLY, BRETT
To: LAWRENCE LIVERMORE NATIONAL SECURITY, LLC
Reel/Frame 053254/0526 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2020
From: TAYLOR, HAYDEN K.; BHATTACHARYA, INDRASEN; HEIDARI, HOSSEIN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 053254/0579 →
Continuity (2)
Provisional Application 62847199 · May 13, 2019
Related Publication 20200361152A1 · Nov 19, 2020