IP Library › Granted Patent US 10,703,859
Granted Patent B2
US 10,703,859 · App. 15/982,627 · Granted Jul 7, 2020

Compositions comprising unsaturated crystalline polyester for 3D printing

Inventors: Shivanthi E. Sriskandha (Mississauga, CA); Valerie M. Farrugia (Oakville, CA); Guerino G. Sacripante (Oakville, CA); Edward G. Zwartz (Mississauga, CA)
Assignee: XEROX CORPORATION
C08G63/52C08F2/22C08F22/02C08G81/027B33Y70/00C08F2500/17C08F2800/10
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,703,859
App. No.
15/982,627
Filed
May 17, 2018
Granted
Jul 7, 2020
Kind
B2
Examiner
LEE, RIP A
Art Unit
1762
USPC
526/318.2
Abstract

A composition for use in 3D printing includes an unsaturated polyester resin including an ethylenically unsaturated monomer, a first diol monomer and a second diol monomer.

Claims (23)

1. A three-dimensional (3D) printing composition comprising:

an unsaturated polyester resin having a particle circularity of from about 0.910 to about 0.940 and a thermal initiator combined to form cured and crosslinked unsaturated polyester resin particles, the unsaturated polyester resin comprising

an ethylenically unsaturated monomer having the formula I

wherein each p and q is independently from 0 to 8, and z is 1 to 5,

a first diol monomer; and

a second diol monomer, wherein the cured and crosslinked unsaturated polyester resin comprises from about 75% to about 100% by weight of the composition.

2. The composition of claim 1 , wherein the ethylenically unsaturated monomer is selected from the group consisting of maleic acid, fumaric acid, 3-hexenedioic acid, 2-heptenedioic acid, 2-octenedioic acid, glutaconic acid, 2-decenedioic acid, traumatic acid, muconic acid, and mixtures thereof.

3. The composition of claim 1 , wherein the ethylenically unsaturated monomer is present from about 49 to about 51 mole percent (mol %) of the unsaturated polyester resin.

4. The composition of claim 1 , wherein the first diol monomer is present from about 30 to about 45 mole percent (mol %) of the unsaturated polyester resin.

5. The composition of claim 1 , wherein the second diol monomer is present from about 25 to about 40 mole percent (mol %) of the unsaturated polyester resin.

6. The composition of claim 1 , wherein a molar ratio of the first diol monomer to the second diol monomer is from about 80:20 to about 60:50.

7. The composition of claim 1 , wherein the unsaturated polyester resin has a crystallization temperature (Tc) of from about 50° C. to about 70° C.

8. The composition of claim 1 , wherein the unsaturated polyester resin has a melting temperature (Tm) of from about 75° C. to about 110° C.

9. The composition of claim 1 , wherein the unsaturated polyester resin has a viscosity at 120° C. from about 200 to 600 Poise.

10. The composition of claim 1 , wherein the acid value of the unsaturated polyester resin is from about 3 to 20 mg KOH/g.

11. A method of making a three-dimensional (3D) printing composition, comprising:

copolymerizing a mixture comprising an ethylenically unsaturated dicarboxylic acid, a first diol, and a second diol, thereby forming an unsaturated polyester resin, wherein the copolymerizing is conducted at a temperature in a range from about 150° C. to about 205° C.;

dispersing the unsaturated polyester resin with a solution comprising a surfactant to form a resin emulsion; and

contacting the resin emulsion with a thermal initiator to form a cross-linked polyester resin, wherein the cross-linked polyester resin comprises from about 75% to about 100% by weight of the three-dimensional (3D) printing composition.

12. The method of claim 11 , wherein the contacting the unsaturated polyester resin is performed in the absence of a solvent.

13. The method of claim 11 , wherein a molar ratio of the first diol to the second diol is from about 75:25 to about 65:35.

14. The method of claim 11 , wherein the thermal initiator is selected from the group consisting of ammonium persulfate, sodium persulfate, potassium persulfate, organic peroxides, 2,2′-azobis(2-methylpropanenitrile), 1,1′-azobis(cyanocyclohexane), 2-methyl-2,2′-azobis propanenitrile, 2-2′-azobis isobutyramide dihydrate 2, 2′-azobis(2-methyl-N-phenylpropionamidine) dihydrochloride, 2,2′-azobis[N-(4-chlorophenyl)-2-methylpropionamidine]dihydrochloride, 2,2′-azobis[N-(4-hydroxyphenyl)-2-methyl-propionamidine]dihydrochloride, 2,2′-azobis[N-(4-amino-phenyl)-2-methylpropionamidine]tetrahydrochloride, 2,2′-azobis[2-methyl-N(phenylmethyl)propionamidine]dihydrochloride, 2,2′-azobis[2-methyl-N-2-propenylpropionamidine]dihydrochloride, 2,2′-azobis[N-(2-hydroxy-ethyl)-2-methylpropionamidine]dihydrochloride, 2,2′-azobis[2(5-methyl-2-imidazolin-2-yl)propane]dihydrochloride, 2,2′-azobis[2-(2-imidazolin-2-yl)propane]dihydrochloride, 2,2′-azobis[2-(4,5,6,7-tetrahydro-1H-1,3-diazepin-2-yl)propane]dihydrochloride, 2,2′-azobis[2-(3,4,5,6-tetrahydropyrimidin-2-yl)propane]dihydrochloride, 2,2′-azobis[2-(5-hydroxy-3,4,5,6-tetrahydropyrimidin-2-yl)propane]dihydrochloride, 2,2′-azobis {2-[1-(2-hydroxyethyl)-2-imidazolin-2-yl]propane}dihydrochloride, and mixtures thereof.

15. The method of claim 11 further comprising sintering the composition to build a 3D object.

Assignments (10)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2025
From: XEROX CORPORATION
To: GENESEE VALLEY INNOVATIONS, LLC
Reel/Frame 073562/0677 →
SECOND LIEN NOTES PATENT SECURITY AGREEMENT Recorded Jul 2, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 071785/0550 →
FIRST LIEN NOTES PATENT SECURITY AGREEMENT Recorded Apr 11, 2025
From: XEROX CORPORATION
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 070824/0001 →
SECURITY INTEREST Recorded Feb 13, 2024
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 066741/0001 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT RF 064760/0389 Recorded Feb 13, 2024
From: CITIBANK, N.A., AS COLLATERAL AGENT
To: XEROX CORPORATION
Reel/Frame 068261/0001 →
SECURITY INTEREST Recorded Nov 20, 2023
From: XEROX CORPORATION
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 065628/0019 →
SECURITY INTEREST Recorded Jun 22, 2023
From: XEROX CORPORATION
To: CITIBANK, N.A., AS COLLATERAL AGENT
Reel/Frame 064760/0389 →
RELEASE OF SECURITY INTEREST IN PATENTS AT R/F 062740/0214 Recorded May 18, 2023
From: CITIBANK, N.A., AS AGENT
To: XEROX CORPORATION
Reel/Frame 063694/0122 →
SECURITY INTEREST Recorded Nov 10, 2022
From: XEROX CORPORATION
To: CITIBANK, N.A., AS AGENT
Reel/Frame 062740/0214 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2018
From: SRISKANDHA, SHIVANTHI E.; FARRUGIA, VALERIE M.; SACRIPANTE, GUERINO G.; ZWARTZ, EDWARD G.
To: XEROX CORPORATION
Reel/Frame 045836/0648 →
Continuity (1)
Related Publication 20190352455A1 · Nov 21, 2019