IP Library Granted Patent US 8,334,025
Granted Patent B2
US 8,334,025 · App. 12/092,490 · Granted Dec 18, 2012

Antimony-free photocurable resin composition and three dimensional article

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Quick Facts
Patent No.
US 8,334,025
App. No.
12/092,490
Granted
Dec 18, 2012
Kind
B2
Abstract

The present invention provides a low viscosity photocurable composition including (i) a cationically curable component (ii) a free radically active component (iii) an antimony-free cationic photoinitiator (v) a free radical photoinitiator, and (vi) a toughening agent. The photocurable composition can be cured using rapid prototyping techniques to form three-dimensional articles which can be used in various aerospace and investment casting applications.

Claims (56)

1. A photocurable composition comprising:

(a) 35-80% by weight of a cationically curable component;

(b) 15-60% by weight of a free radically active component;

(c) 0.1-10% by weight of an antimony-free cationic photoinitiator;

(d) 0-10% by weight of a free radical photoinitiator; and

(e) 0-40% by weight of one or more toughening agents

wherein the percent by weight is based on the total weight of the photocurable composition, the free radically active component comprises at least one dendritic polymer acrylate compound, and the photocurable composition has a viscosity of less than 500 cps.

2. The photocurable composition of claim 1 wherein the free radically active component comprises a poly(meth)acrylate.

3. The photocurable composition of claim 2 wherein the poly(meth)acrylate comprises a difunctional acrylate compound.

4. The photocurable composition of claim 2 wherein the free radically active component further comprises an epoxy functionalized compound.

5. The photocurable composition of claim 1 wherein the cationically curable component comprises a hydrogenated bisphenol epoxy-containing compound.

6. The photocurable composition of claim 5 wherein the cationically curable component further comprises an oxetane compound.

7. The photocurable composition of claim 1 wherein the antimony-free cationic photoinitiator is a triarylsulfonium hexafluorophosphate salt.

8. The photocurable composition of claim 1 wherein the photocurable composition comprises 0.01-40% by weight of one or more toughening agents.

9. The photocurable composition of claim 8 wherein the toughening agent comprises reactive particles comprising a polysiloxane core and a shell containing reactive groups.

10. The photocurable composition of claim 1 wherein the photocurable composition has a viscosity in the range of 50-500 cps.

11. The photocurable composition of claim 1 wherein the photocurable composition, after cure by exposure to actinic radiation and optionally heat, has a notched izod impact between 0.6 ft. lbs/in and 1.1 ft. lbs/in.

12. The photocurable composition of claim 1 wherein the photocurable composition, after cure by exposure to actinic radiation and optionally heat, has a notched izod impact of at least 0.6 ft. lbs/in.

13. A photocurable composition comprising:

(a) 35-80% by weight of a cationically curable component;

(b) 1 5-60% by weight of a free radically active component comprising (i) at least one poly(meth)acrylate compound and (ii) at least one dendritic polymer acrylate compound;

(c) 0.1-10% by weight of an antimony-free cationic photoinitiator;

(d) 0-10% by weight of a free radical photoinitiator;

(e) 0-40% by weight of one or more toughening agents

wherein the percent by weight is based on the total weight of the photocurable composition and wherein the photocurable composition, after cure by exposure to actinic radiation and optionally heat has at least one of a tensile strength of at least 30 MPa, a flexural modulus within the range from about 1000-2300 MPa, a notched izod impact of at least 0.6 ft, lbs/in, and/or an average elongation at break of at least 5%.

14. The photocurable composition of claim 13 wherein the photocurable composition comprises 0.01-40% by weight of one or more toughening agents and the photocurable composition, after cure by exposure to actinic radiation and optionally heat, has a notched izod impact of at least 0.6 ft. lbs/in.

15. The photocurable composition of claim 13 wherein the poly(meth)acrylate comprises a difunctional acrylate compound.

16. The photocurable composition of claim 13 wherein the free radically active component further comprises an epoxy functionalized compound.

17. The photocurable composition of claim 13 wherein the cationically curable component comprises a hydrogenated bisphenol epoxy-containing compound.

18. The photocurable composition of claim 17 wherein the cationically curable component further comprises an oxetane compound.

19. The photocurable composition of claim 13 wherein the photocurable composition comprises 0.01-40% by weight of one or more toughening agents.

20. A process for producing a non-toxic photocurable composition comprising mixing together

(a) 35-80% by weight of a cationically curable component;

(b) 15-60% by weight of a free radically active component comprising (i) at least one poly(meth)acrylate compound and (ii) at least one dendritic polymer acrylate compound;

(c) 0.1-10% by weight of an antimony-free cationic photoinitiator;

(d) 0-10% by weight of a free radical photoinitiator; and optionally

(e) 0-40% by weight of one or more toughening agents,

wherein the photocurable composition has a viscosity of less than 500 cps.

21. A process for producing an antimony-free three dimensional article comprising:

(a) forming a first layer of the photocurable composition of claim 1 on a surface;

(b) exposing the layer imagewise to actinic radiation to form an imaged cross-section, wherein the radiation is of sufficient intensity to cause substantial curing of the layer in the exposed areas;

(c) forming a second layer of the composition of claim 1 on the previously exposed imaged cross-section;

(d) exposing the second layer from step (c) imagewise to actinic radiation to form an additional imaged cross-section, wherein the radiation is of sufficient intensity to cause substantial curing of the second layer in the exposed areas and to cause adhesion to the previously exposed imaged cross-section; and

(e) repeating steps (c) and (d) a sufficient number of times in order to build up the three-dimensional article.

22. The process of claim 21 wherein the photocurable composition comprises 0.01-40% by weight of one or more toughening agents, preferably a toughening agent comprising reactive particles having a polysiloxane core and a shell containing reactive groups.

23. The process of claim 22 wherein the photocurable composition has a viscosity in the range of 50-500 cps.

24. A three-dimensional medical article produced according to the process of claim 21 .

25. The three-dimensional medical article of claim 24 wherein the medical article is a medical device, medical model or medical implant, successfully meeting the requirements of USP 28, NF 23, for the biological tests for plastics, class VI, 70° C.

26. An antimony-free three-dimensional article produced by the process of claim 21 .

27. A process for producing a three dimensional article by jet printing comprising the steps of:

(a) applying successive droplets of the photocurable composition of claim 1 at targeted locations on a substrate in accordance with a desired shape stored on a computer file;

(b) exposing the droplets to electromagnetic radiation to cure the droplets in the exposed areas;

(c) repeating steps (a) and (b) a sufficient number of times in order to build up the three dimensional article.

28. The process of claim 27 wherein the substrate comprises paper, textiles, tiles, printing plates, wallpaper, plastic, powder, paste or a reactive resin, liquid or already partly cured.

29. The process of claim 27 wherein the photocurable composition is exposed to electromagnetic radiation pixel by pixel, line by line, layer by layer, after several layers have been formed, and/or after all layers have been formed.

30. The process of claim 27 wherein the electromagnetic radiation employed is UV light, microwave radiation, visible light, or laser beams.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Aug 26, 2021
From: HSBC BANK USA, NATIONAL ASSOCIATION
To: 3D SYSTEMS, INC.
Reel/Frame 057651/0374 →
SECURITY INTEREST Recorded Feb 27, 2019
From: 3D SYSTEMS, INC.
To: HSBC BANK USA, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 048456/0017 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2012
From: HUNTSMAN INTERNATIONAL LLC
To: 3D SYSTEMS, INC.
Reel/Frame 027861/0128 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2011
From: FONG, JOHN WAI; LEYDEN, RICHARD N.; MESSE, LAURENCE; PATEL, RANJANA C.; CHAPELAT, CAROLE
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 026992/0318 →