IP Library Granted Patent US 9,808,993
Granted Patent B2
US 9,808,993 · App. 14/637,070 · Granted Nov 7, 2017

Method for solid freeform fabrication

Inventors: Andrew J. Boydston (Seattle, WA); Mark Ganter (Edmonds, WA); Duane Storti (Seattle, WA); Adam Edward Goetz (Seattle, WA); Mete Yurtoglu (Seattle, WA); Michael Byrnes Larsen (Seattle, WA); Gregory Isaac Peterson (Tacoma, WA)
Assignees: Ricoh Co., Ltd.; University of Washington
B29C67/0066B29B13/021B29C67/0081B29C67/0088B29C71/0009B29K2079/08B29K2105/251B33Y10/00B33Y30/00B33Y50/02B33Y70/00
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Quick Facts
Patent No.
US 9,808,993
App. No.
14/637,070
Granted
Nov 7, 2017
Kind
B2
Abstract

The present invention provides methods, processes, and systems for the manufacture of three-dimensional articles made of polymers using 3D printing. A layer of prepolymer is deposited on a build plate to form a powder bed. The deposited powder bed is heated to about 50° C. to about 170° C. Then, a solution of activating agent is printed on the powder bed in a predetermined pattern, and a stimulus is applied converting the prepolymer to the final polymer. After a predetermined period of time, sequential layers are printed to provide the three-dimensional article. The three-dimensional object can be cured to produce the three-dimensional article composed of the final polymers.

Claims (17)

1. A method for manufacturing a three-dimensional article, the method comprising:

a. depositing a powder of prepolymer on a build plate to form a powder bed;

b. printing a solution of an activating agent at selected locations on the powder bed;

c. exposing the printed solution to a stimulus to form a polymer layer of the three-dimensional article; and

d. repeating steps (a)-(c) to manufacture remainder of the three-dimensional article.

2. The method of claim 1 , wherein the prepolymer is poly(amic acid), polysulfide, ketalized version of a polyketone, or a reduced form a polyketone.

3. The method of claim 2 , wherein the poly(amic acid) comprises an aromatic dianhydride and an aromatic diamine.

4. The method of claim 3 , wherein the aromatic dianhydride and the aromatic diamine are in about 1:1 molar ratio.

5. The method of claim 3 , wherein the aromatic dianhydride is selected from the group consisting of pyromellitic dianhydride (PMDA), biphenyl dianhydride (BPDA), benzophenonetetracarboxylic dianhydride (BTDA), and combination thereof.

6. The method of claim 3 , wherein diamine is p-phenylenediamine (PDA), 4,4′-oxydianiline (ODA), or combinations thereof.

7. The method of claim 1 , wherein step b further comprises heating the powder bed to about 50° C. to about 170° C.

8. The method of claim 1 , wherein the activating agent is acetic anhydride, pyridine, triethylamine, N-methyl-pyrrolidine, or combinations thereof.

9. The method of claim 1 , wherein stimulus comprises heat, light, oxidation, acid catalysis, base catalysis, transition metal catalysis, or combination thereof.

10. The method of claim 1 , wherein the steps are repeated after about 5 minutes to about 15 minutes.

11. The method of claim 1 , further comprising the step of curing.

12. The method of claim 11 , wherein curing is done by chemical curing or thermal curing.

13. The method of claim 12 , wherein the thermal curing is carried out at about 300° C. or above.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2015
From: BOYDSTON, ANDREW J.; GANTER, MARK; STORTI, DUANE; GOETZ, ADAM EDWARD; YURTOGLU, METE; LARSEN, MICHAEL BYRNES; PETERSON, GREGORY ISAAC
To: RICOH COMPANY, LTD.; UNIVERSITY OF WASHINGTON
Reel/Frame 035567/0433 →
Continuity (1)
Related Publication 20160257070A1 · Sep 8, 2016