IP Library Granted Patent US 12,709,697
Granted Patent B2
US 12,709,697 · App. 18/034,458 · Granted Aug 18, 2026

(meth)acrylate-functional radiation curable compositions for additive fabrication

Inventor: Govindarajan Sudhanva (Elgin, IL)
Assignee: Stratasys, Inc.
C09D175/14C08G18/04C08G18/12
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Quick Facts
Patent No.
US 12,709,697
App. No.
18/034,458
Filed
Apr 28, 2023
Granted
Aug 18, 2026
Kind
B2
Art Unit
1765
USPC
522/64
Abstract

Described herein are thermoset compositions and kits of compositions suitable for use in additive fabrication processes including specified concentrations of reactive compounds including urethane-(meth)acrylate compounds, monofunctional diluent monomers, and methacrylate-functional compounds having 1.5 polymerizable groups or more. Also described and claimed are methods of creating three-dimensional parts via additive fabrication processes utilizing the compositions elsewhere herein described and claimed, as well as the articles cured therefrom.

Claims (29)

1 . A radiation curable composition for additive fabrication comprising, relative to the entire weight of the composition:

from 40 to 95 wt. %, based on the total weight of the composition, of a (i) urethane (meth)acrylate oligomer having at least one polymerizable group,

wherein the urethane (meth)acrylate oligomer is the reaction product of a diisocyanate, a polyether polyol, and a hydroxy-functional (meth)acrylate;

from 0 to less than 40 wt. % of (ii) a monofunctional reactive diluent monomer;

greater than 20 wt. % of (iii) one or more methacrylate-functional compounds comprising a number average of greater than 1.5 polymerizable groups;

wherein at least one of the polymerizable groups of the compound according to (iii) is (co)polymerizable with the at least one polymerizable group of the oligomer according to (i) and/or (ii); and

wherein the compound according to (iii) possesses a number average molecular weight (Mn) value that is less than the Mn value of the oligomer according to (i) and greater than the Mn of the monomer according to (ii);

wherein Mn is measured by size exclusion chromatography (SEC) method.

2 . The radiation curable composition according to claim 1 , further comprising, relative to the weight of the entire composition,

from 0.5 to 8 wt. % of one or more photoinitiators; and/or

from 1 to 40 wt. % of one or more additives; wherein the additives further comprise fillers and/or impact modifiers.

3 . The radiation curable composition according to claim 1 , wherein the urethane (meth)acrylate oligomer (i) possess an Mn value from 750 to 10000 g/mol; and/or

wherein the compound(s) according to (iii) possess an Mn value of less than 750 g/mol and a number average from 1.9 to 3.1, or from 1.9 to 2.1 polymerizable groups.

4 . The radiation curable composition according to claim 1 , wherein the oligomer(s) according to (i) possesses an uncured Tg, as measured by differential scanning calorimetry, from −50 to 10° C.; and/or wherein the oligomer(s) according to (i) possess a number average from 0.9 to 2.1, or from 1.9 to 2.1 polymerizable groups.

5 . The radiation curable composition according to claim 1 , wherein the oligomer(s) according to (i) are present by weight, relative to the entire composition, from 50 to 95 wt. %.

6 . The radiation curable composition according to claim 1 , wherein the oligomer(s) according to (i) comprises the reaction product of isophorone diisocyanate, hexane diisocyanate, 2,2,4-trimethyl hexane diisocyanate, 2,4,4-trimethylhexane diisocyanate, pentane diisocyanate or 4,4-methylene bis(cyclohexyl isocyanate), or mixtures thereof;

and/or

wherein the oligomer(s) according to (i) comprise the reaction product of a polyol having an Mn from 200 to 6000 g/mol, wherein the polyol comprises polyethylene glycol, polypropylene glycol, poly THF, polybutylene oxide, polyethylene co-propylene oxide, or polyethylene oxide-block-propylene oxide, or mixtures thereof.

7 . The radiation curable composition according to claim 1 , wherein the oligomer(s) according to (i) comprise the reaction product of hydroxy ethyl methacrylate, 1-hydroxypropyl methacrylate, 2-hydroxypropyl methacrylate, 1-hydroxybutyl methacrylate, diethylene glycol methacrylate, dipropylene glycol methacrylate, or caprolactone 2-(methacryloyloxy) ethyl ester, or mixtures thereof.

8 . The radiation curable composition according to claim 1 , wherein the polymerizable groups comprises acrylate groups.

9 . The radiation curable composition according to claim 1 , wherein the compound(s) according to (ii) comprises monofunctional urethane methacrylates.

10 . The radiation curable composition according to claim 1 , wherein the compound(s) according to (ii) comprises isopropylideneglycerol methacrylate (IPGMA), (hydroxyethyl) methacrylate (HEMA), 2-hydroxypropyl methacrylate (HPMA), benzyl methacrylate (BMA), cyclohexyl methacrylate, isobornyl methacrylate, or 4-tbutylcyclohexyl methacrylate, THFmethacrylate, phenyl methacrylate, 2,2,4-trmethylcyclohexyl methacrylate, or mixtures thereof.

11 . The radiation curable composition according to claim 10 , wherein the compound(s) according to (iii) comprises bisphenol A glycidyl methacrylate, a triethylene glycol dimethacrylate, a trimethylhexamethylene diisocyanate di(hydroxyethyl) methacrylate, or a methacrylate-terminated isocyanate comprising a methacrylate-terminated moiety and an isocyanate moiety, or mixtures thereof.

12 . The radiation curable composition according to claim 1 , wherein the compound(s) according to (iii) comprises difunctional compounds having a number average molecular weight from 150 to 750 g/mol; and/or

wherein the compound(s) according to (iii) are present, relative to the weight of the entire composition, from 15 to 55 wt. %.

13 . The radiation curable composition according to claim 1 , wherein the polymerizable groups in the compound(s) according to (i) consist of acrylate groups, and wherein the polymerizable groups in the compound(s) according to (iii) consist of methacrylate groups.

14 . The radiation curable composition according to claim 1 , wherein the composition contains from 0 to 0.1 equivalents of acrylate groups; and/or

from 0.2 to 0.3 equivalents of methacrylate groups.

15 . The method according to claim 1 , wherein a linear polymer formed from the oligomer(s) according to (i) has a Tg between-80 to 20° C.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 13, 2023
From: COVESTRO (NETHERLANDS) B.V.
To: STRATASYS, INC.
Reel/Frame 065216/0498 →
Continuity (2)
Provisional Application 63106382 · Oct 28, 2020
Related Publication 20230407132A1 · Dec 21, 2023
References Cited (7)
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WO 2019204807A1 · 2019 [cited by applicant]
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International Written Opinion, ISA/EP, PCT/EP2021/079885, dated Feb. 16, 2022, 6 pages. [cited by applicant]