Photo-curable compositions containing high refractive index monomers for use in 3D printing applications
Disclosed are high refractive index monomers for ceramic/metal 3D printing applications. The compositions disclosed herein have a higher refractive index and thus better resolution and lower scattering of the light when employed in a composition to deposit ceramic or metallic particles. The disclosed compositions also include low refractive cross-linkers selected for their good thermal decomposition and reactivity to provide good cohesion during the 3D printing.
1 . A photo-curable composition for use in a composition suitable for three-dimensional printing, the photo-curable composition comprising:
a. a monomer composition comprising at least one monomer having a refractive index of at least 1.49, wherein the at least one monomer is selected from the group consisting of
i. at least one monomer selected from the group consisting of poly(oxy-1,2-ethanediyl), alpha-(1-oxo-2-propen-1-yl)-omega-(4-(1-methyl-1-phenylethyl)phenoxy)-, N-vinyloxazole, and N-vinylcarbazole,
ii. at least one monomer of Formula I
wherein,
Z is an ethylenically unsaturated group; X is O, S, or NH; L 1 and L 2 are each independently C 1 -C 3 alkylene, —(C 1 -C 3 alkylene)-S—(C 1 -C 3 alkylene)-, or —(C 1 -C 3 alkylene)-O—(C 1 -C 3 alkylene)-; R is hydrogen or C 1 -C 6 alkyl; R 1 and R 2 are each independently aryl, aryl (C 1 -C 6 alkylene)-, heteroaryl, or heteroaryl (C 1 -C 6 alkylene)-, each of which group is substituted with 0 to 5 substituents independently selected from halogen, C 1 -C 4 alkyl, C 1 -C 4 alkoxy, (C 1 -C 4 alkyl)S—, C 1 -C 4 haloalkyl, and C 1 -C 4 haloalkoxy; and Y 1 and Y 2 are each independently O, S, NH, or N,
iii. at least one monomer of Formula II
wherein,
A is H or CH3, and
Q is selected from the group consisting of ethylene glycol phenyl ether, poly(ethylene glycol phenyl ether acrylate), phenyl, hexylphenoxy, hexylphenoxy, 2-phenylethyl, 4-methylphenyl, 4-methylbenzyl, 2-2-methyphenylethyl, 2-3-methylphenylethyl, 2-4-methylphenylethyl, 2-(4-propylphenyl) ethyl, 2-(4-(1-methylethyl)phenyl)ethyl, 2-(4-methoxyphenyl)ethyl, 2-(4-chlorophenyl) ethyl, 2-(2-chlorophenyl)ethyl, 2-(3-chlorophenyl)ethyl, 2-(4-chlorophenyl) ethyl, 2-(4-bromophenyl)ethyl, 2-(3-phenylphenyl)ethyl, 2-(4-phenylphenyl) ethyl), and 2-(4-benzylphenyl)ethyl or Q is a moiety that includes at least one substituted or unsubstituted heteroaromatic ring,
iv. at least one monomer of formula III,
wherein
A is H or Me,
L is a bond, C 1 -C 3 alkylene or —(CR c R d —CR′ c R′ d —O) m ;
each R c , R d , R′ c and R′ d is independently H or alkyl;
m is 2 to 10; and
Q′ corresponds to one of the following formulae:
wherein the symbol ● corresponds to the point of attachment to linker L;
b. a cross-linker; and
c. a plasticizer.
2 . The photo-curable composition of claim 1 , wherein the monomer having a refractive index of at least 1.49 is at least one selected from the group consisting of poly(oxy-1,2-ethanediyl), alpha-(1-oxo-2-propen-1-yl)-omega-(4-(1-methyl-1-phenylethyl)phenoxy)-, N-vinyloxazole and N-vinylcarbazole.
3 . The photo-curable composition of claim 1 , wherein the monomer having a refractive index of at least 1.49 is the at least one acrylate monomer of Formula I wherein Z is acryloyl or methacryloyl.
4 . The photo-curable composition of claim 3 , wherein the monomer of formula I is selected from the group consisting of 1,3-bis(2-bromophenoxy)propan-2-yl acrylate, 1,3-bis(4-bromophenoxy)propan-2-yl acrylate, 1,3-bis(3-bromophenoxy)propan-2-yl acrylate, 1,3-bis(4-methylphenylthio)-2-propyl acrylate, 1,3-bis(phenoxy)propan-2-yl acrylate, 1,3-bis(2-mercaptobenzothiazoyl)-2-propyl acrylate, 1,3-bis(benzo[d]thiazol-2-ylthio)propan-2-yl acrylate, 1,3-bis(2,4,6-tribromophenoxy)-2-propyl acrylate, 1,3-bis(phenylthio)propan-2-yl acrylate, 1,3-bis(4-bromophenylthio)propan-2-yl acrylate, 1,3-bis(3-bromophenylthio)propan-2-yl acrylate, 1,3-bis(2,4,6-tribromophenylthio)propan-2-yl acrylate, 1,3-di(10H-phenothiazin-10-yl)propan-2-yl acrylate, 1,3-bis(2-(phenylthio)ethylthio)propan-2-yl acrylate, 1-phenoxy-3-(phenylthio)propan-2-yl acrylate, 1-(4-chlorophenoxy)-3-(phenylthio)propan-2-yl acrylate, 1-(4-bromophenoxy)-3-(4-bromophenylthio)propan-2-yl acrylate, 1-(2,4,6-tribromophenoxy)-3-(2,4,6-tribromophenylthio)propan-2-yl acrylate, and 1-(2,4-dibromophenoxy)-3-(2,4-dibromophenylthio)propan-2-yl acrylate, and mixtures thereof.
5 . The photo-curable composition of claim 1 , wherein the monomer having a refractive index of at least 1.49 is the at least one monomer of Formula II.
6 . The photo-curable composition of claim 5 , wherein the monomer of formula II is selected from the group consisting of poly(ethylene glycol) phenyl ether acrylate (polyEGPEA), phenyl methacrylate, hexylphenoxy methacrylate, hexylphenoxy acrylate, 2-phenylethyl methacrylate, 4-methylphenyl methacrylate, 4-methylbenzyl methacrylate, 2-(2-methylphenyl)ethyl methacrylate, 2-(3-methylphenyl)ethyl methacrylate, 2-(4-methylphenyl)ethyl methacrylate, 2-(4-propylphenyl)ethyl methacrylate, 2-(4-(1-methylethyl)phenyl)ethyl methacrylate, 2-(4-methoxyphenyl)ethyl methacrylate, 2-(4-cyclohexylphenyl)ethyl methacrylate, 2-(2-chlorophenyl)ethyl methacrylate, 2-(3-chlorophenyl)ethyl methacrylate, 2-(4-chlorophenyl)ethyl methacrylate, 2-(4-bromophenyl)ethyl methacrylate, 2-(3-phenylphenyl)ethyl methacrylate, 2-(4-phenylphenyl)ethyl methacrylate), 2-(4-benzylphenyl)ethyl methacrylate, 2-(phenylphenoxy)ethyl acrylate, 2-phenoxyethyl acrylate, 2-(phenylthio)ethyl (meth)acrylate, (2-phenoxy-2-phenyl)ethyl (meth)acrylate, (2-phenyl-2-phenylthio)ethyl (meth)acrylate, 2-, 3-, and 4-bromophenyl (meth)acrylate, 2,4,6-tribromophenyl (meth)acrylate, tetrabromophenyl (meth)acrylate, pentabromophenyl (meth)acrylate, 2-, 3-, and 4-bromobenzyl (meth)acrylate, 2,4,6-tribromobenzyl (meth)acrylate, tetrabromobenzyl (meth)acrylate, pentabromobenzyl (meth)acrylate, 3-phenyl-2-hydroxypropyl (meth)acrylate, ortho-biphenyl (meth)acrylate, 3-(2,4-dibromophenyl)-2-hydroxypropyl (meth)acrylate, (2-hydroxy-3-phenoxy)propyl (meth)acrylate, and mixtures thereof.
7 . The photo-curable composition of claim 1 , wherein the monomer having a refractive index of at least 1.49 is the at least one monomer of formula III.
8 . The photo-curable composition of claim 7 , wherein the monomer having a refractive index of at least 1.49 comprises mono(meth)acrylate of tricyclodecane methanol of formula
wherein A is H or CH 3 .
9 . The photo-curable composition of claim 1 , wherein the cross-linker has at least two ethylenically unsaturated groups.
10 . The photo-curable composition of claim 1 , wherein the cross-linker is selected from the group consisting of ethylene glycol di(meth)acrylate, 1,2-propanediol di(meth)acrylate, 1,3-propanediol di(meth)acrylate, 1,4-butanediol di(meth)acrylate, 1,3-butanediol di(meth)acrylate, 1,5-pentanediol di(meth)acrylate, 1,6-hexanediol di(meth)acrylate, 1,10-decanediol di(meth)acrylate, 1,12-dodecanediol di(meth)acrylate, diethylene glycol di(meth)acrylate, triethylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, poly(ethylene glycol) di(meth)acrylate, dipropylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, tetrapropylene glycol di(meth)acrylate, poly(propylene glycol) di(meth)acrylate, neopentyl glycol di(meth)acrylate, cyclohexane dimethanol di(meth)acrylate, bisphenol A di(meth)acrylate, hydrogenated bisphenol A di(meth)acrylate, tricyclodecane dimethanol di(meth)acrylate, trimethylolpropane tri(meth)acrylate, triethylolpropane tri(meth)acrylate, glycerol tri(meth)acrylate, pentaerythritol tetra(meth)acrylate, an aromatic urethane oligomer having 2 to 6 (meth)acrylate groups, and mixtures thereof.
11 . The photo-curable composition of claim 1 , wherein the plasticizer is selected from the group consisting of dialkyl phthalates, alkyl phosphates, poly(ethylene glycol), polyethylene glycol esters, polyethylene glycol ethers, polybutadiene, polybutadiene styrene copolymers, polyisoprenes, glycerol, and mixtures thereof.
12 . The photo-curable composition of claim 1 , wherein the plasticizer is poly(ethylene glycol).
13 . The photocurable composition according to 1, wherein the photocurable composition comprises
from about 5 wt. % to about 40 wt. % based on the total weight of the photo-curable composition of monomer composition a);
from about 20 wt. % to about 65 wt. % based on the total weight of the photo-curable composition of cross-linker b); and
from about 20 wt. % to about 65 wt. % based on the total weight of the photo-curable composition of plasticizer c).
14 . A photo-curable ink composition suitable for use in 3D printing, the ink composition comprising:
a photo-curable composition as defined in claim 1 ;
a photo-initiator;
scaffold particles; and
a dispersant.
15 . The photo-curable ink composition of claim 14 , wherein the scaffold particles are selected from the group consisting of a metallic powder, a ceramic powder, graphite powder, graphene powder, diamond powder, carbide powder, silicide powder, nitride powder, oxide powder, graphene, carbon nanofiber, carbon nanotubes, zirconia, and mixtures thereof.
16 . The photo-curable ink composition of claim 14 , wherein the photo-initiator is selected from the group consisting of diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide, Bis(2,4,6-trimethylbenzoyl)-phenylphosphineoxide, 2-hydroxy-2-methyl-1-phenyl-1-propane, benzophenone, and mixtures thereof.
17 . The photo-curable ink composition of claim 14 , wherein the photo-curable ink composition comprises:
from about 20 wt. % to about 50 wt. % based on the total weight of the ink composition of the photo-curable composition;
from about 0.01 wt. % to about 5.0 wt. % based on the total weight of the ink composition of the photo-initiator;
from about 50 wt. % to about 80 wt. % based on the total weight of the ink composition of the scaffold particles; and
from about 0.2 wt. % to about 4.0 wt. % based on the total weight of the ink composition of the dispersant.
18 . A method of making an inorganic structure, the method comprising
(i) obtaining a photo-curable ink composition as defined in claim 14 ;
(ii) polymerizing and 3D-printing at least a portion of the photo-curable ink composition to generate a pre-inorganic polymer; and
(iii) thermally treating at least a portion of the pre-inorganic polymer to produce an inorganic structure.