IP Library Granted Patent US 12,473,254
Granted Patent B2
US 12,473,254 · App. 17/995,834 · Granted Nov 18, 2025

Photocurable polymer compositions

Inventors: Joel Pollino (Johns Creek, GA); Kermit S. Kwan (Cumming, GA); Timothy Long (Blacksburg, VA); Christopher Williams (Blacksburg, VA); Viswanath Meenakshisundaram (Blacksburg, VA); Cody Weyhrich (Christiansburg, VA)
Assignees: VIRGINIA TECH INTELLECTUAL PROPERTIES, INC.; SOLVAY SPECIALTY POLYMERS USA, LLC
C07C317/24B33Y10/00G03F7/0037G03F7/2002
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Quick Facts
Patent No.
US 12,473,254
App. No.
17/995,834
Granted
Nov 18, 2025
Kind
B2
Abstract

The present invention relates to relates to a polymer formulation for three-dimensionally (3D) printing an article by stereolithography, the formulation comprising a functionalized polymer. The invention further relates to lithographic methods to form 3D objects that incorporate the aforementioned polymer formulation.

Claims (44)

1 . A polymer formulation (F) comprising, based on the total weight of the formulation (F):

from 1 to 50 wt. %, based on the total weight of F, of at least one poly(aryl ethersulfone) (PAES) polymer (P) comprising at least one terminal group of formula (M1) or (M2):

wherein

R 2 is H or CH 3 ,

X is a bond or (CH 2 )n with n ranging from 1 to 20, and

wherein the number average molecular weight (Mn) of the polymer (P) is of more than 12,000 g/mol, as determined by gel permeation chromatography (GPC) using methylene chloride as a mobile phase and polystyrene standards,

at least one polyfunctional acrylate,

at least one solvent,

optionally at least one photoinitiator, and

optionally at least one blocker,

wherein

wherein the polyfunctional acrylate is according to formula (I):

wherein

R 3 is H or an alkyl having 1 to 5 carbon atoms,

R 4 is according to formula (II):

where n varies between 0 and 10; or

wherein the polyfunctional acrylate is selected from the group consisting of trimethylolpropane propoxytriacrylate, pentaerythritol triacrylate (PETA), glyceryl propoxytriacrylate (GPTA), di(trimethylolpropane) tetraacrylate, glycerol propoxylate triacrylate, pentaerythritol tetraacrylate, 1,3,5-triacryloylhexahydro-1,3,5-triazine, trimethylolpropane trimethacrylate, tris[2-(acryloyloxy)ethyl]isocyanurate, and mixtures thereof.

2 . The formulation (F) of claim 1 , wherein P is a PAES comprising recurring units (R PAES ) of formula (L):

each R 1 is, independently for each aromatic cycle, selected from the group consisting of a halogen, alkyl, alkenyl, alkynyl, aryl, ether, thioether, carboxylic acid, ester, amide, imide, alkali or alkaline earth metal sulfonate, alkyl sulfonate, alkali or alkaline earth metal phosphonate, alkyl phosphonate, amine and quaternary ammonium;

each i is, independently for each aromatic cycle, zero or an integer from 1 to 4;

T is selected from the group consisting of a bond, —CH 2 —; —O—; —SO 2 —; —S—;

—C(O)—; —C(CH 3 ) 2 —; —C(CF 3 ) 2 —; —C(═CCl 2 )—; —C(CH 3 )(CH 2 CH 2 COOH)—; —N═N—; —R a C═CR b —, where each R a and R b , independently from each other, is a hydrogen, a C1-C12-alkyl group, a C1-C12-alkoxy group, a C6-C18-aryl group; —(CH 2 ) m and —(CF 2 ) m with m being an integer from 1 to 6; an aliphatic divalent group, linear or branched, of up to 6 carbon atoms; or a combination thereof.

3 . The formulation (F) of claim 2 , wherein T is selected from the group consisting of a bond, —SO 2 — and —C(CH 3 ) 2 —.

4 . The formulation (F) of claim 2 , wherein the PAES polymer comprises at least 50 mol. % (based on the total number of moles in the polymer) of recurring units of formula (L).

5 . The formulation (F) of claim 2 , wherein the PAES polymer comprises at least 50 mol. % (based on the total number of moles in the polymer) of recurring units selected from the group consisting of formulas:

wherein R 1 is independently for each aromatic cycle, selected from the group consisting of a halogen, alkyl, alkenyl, alkynyl, aryl, ether, thioether, carboxylic acid, ester, amide, imide, alkali or alkaline earth metal sulfonate, alkyl sulfonate, alkali or alkaline earth metal phosphonate, alkyl phosphonate, amine and quaternary ammonium and i is independently for each aromatic cycle, zero or an integer from 1 to 4.

6 . The formulation (F) of claim 1 , comprising at least 0.05 wt. % of polyfunctional acrylate, based on the total weight of the formulation (F).

7 . The formulation (F) of claim 1 , wherein the polyfunctional acrylate is according to formula (III):

8 . The formulation (F) of claim 1 , wherein:

the solvent is selected from the group consisting of N-methylpyrrolidone (NMP), N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMAC), 1,3-dimethyl-2-imidazolidinone (DMI), tetrahydrofuran (THF), dimethyl sulfoxide (DMSO) and sulfolane,

the photoinitiator is selected from the group consisting of 2,2-dimethoxy-2-phenylacetophenone (DMPA), Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide and phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide, and/or

the blocker is selected from the group consisting of avobenzone and 2,5-Bis(5-tert-butyl-benzoxazol-2-yl)thiophene.

9 . A method for manufacturing a 3D article with an additive manufacturing system, comprising:

providing a polymer formulation (F) according to claim 1 , and

printing layers of the 3D article from the polymer formulation (F), and

optionally, curing the 3D article at a temperature ranging from 50 to 450° C.

10 . The method of claim 9 , wherein the step of printing comprises irradiating the polymer formulation (F) with light.

11 . A 3D article obtainable, at least in part, by the method of claim 9 .

12 . A method of manufacturing 3D objects, wherein the method comprises printing the polymer formulation (F) of claim 1 , alone or in combination with other components, and wherein the printing comprises stereolithography (SLA), direct ink writing (DIW), digital light processing (DLP), or inkjet process.

13 . A method of coating an article, the method comprising coating or printing the polymer formulation (F) of claim 1 , alone or in combination with other components.

14 . The formulation (F) of claim 1 , wherein R 3 is H or CH 3 .

15 . The formulation (F) of claim 1 , wherein n is between 0 and 3.

16 . The method of claim 1 , wherein the step of printing comprises irradiating the polymer formulation (F) with UV light or visible light.

17 . The formulation (F) of claim 1 , wherein the polyfunctional acrylate is selected from the group consisting of trimethylolpropane triacrylate (TMPTA), trimethylolpropane ethoxytriacrylate, trimethylolpropane propoxytriacrylate, pentaerythritol triacrylate (PETA), glyceryl propoxytriacrylate (GPTA), di(trimethylolpropane) tetraacrylate, glycerol propoxylate triacrylate, pentaerythritol tetraacrylate, 1,3,5-triacryloylhexahydro-1,3,5-triazine, trimethylolpropane ethoxylate triacrylate, trimethylolpropane ethoxylate triacrylate, trimethylolpropane trimethacrylate, tris[2-(acryloyloxy)ethyl]isocyanurate, and mixtures thereof.

Assignments (3)
CHANGE OF NAME Recorded Oct 14, 2025
From: SOLVAY SPECIALTY POLYMERS USA, LLC
To: SYENSQO SPECIALTY POLYMERS USA, LLC
Reel/Frame 073076/0851 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2024
From: POLLINO, JOEL; KWAN, KERMIT S.
To: SOLVAY SPECIALTY POLYMERS USA, LLC
Reel/Frame 068374/0665 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2024
From: LONG, TIMOTHY; WILLIAMS, CHRISTOPHER; MEENAKSHISUNDARAM, VISWANATH; WEYHRICH, CODY
To: VIRGINIA TECH INTELLECTUAL PROPERTIES, INC.
Reel/Frame 068374/0668 →
Priority Claims (1)
EP 20185769 · Jul 14, 2020 · regional
Continuity (2)
Provisional Application 63007454 · Apr 9, 2020
Related Publication 20230150930A1 · May 18, 2023
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