DARK-COLORED SYSTEM PHOTOPOLYMERIZED COMPOSITION

Abstract

A dark-colored system photopolymerization composition, comprising: 20-80 phr of photopolymerizable prepolymer, 5-60 phr of photopolymerizable monomer, 0.2-8 phr of photoinitiator, and 0.1-5 phr of melanin, 0.05-5 phr of upconversion materials. The composition can construct photopolymerization under near-infrared irradiation. The dark pigment can avoid the strong absorption of near-infrared light, and the upconversion material can absorb near-infrared light with good penetrating ability and emit ultraviolet or visible light to induce the decomposition of free radicals or ionic photoinitiators in the composition. Then produced active species realize the photopolymerization of dark-colored compositions. The invention increases the depth of photopolymerization of dark-colored compositions and improves the mechanical properties of the polymer, that will broaden application fields of photopolymerization materials.

Claims

1. A dark system photopolymerization composition, comprising: photopolymerizable prepolymer 20-80 phr; photopolymerizable prepolymer 20-80 phr; photopolymerizable monomer 5-60 phr; photoinitiator 2-8 phr; dark pigment 1-5 phr; and upconversion materials 0.05-5 phr, wherein: the photoinitiator is selected from the group consisting of 2, 4, 6-trimethylbenzoyl diphenyl phosphine oxide, 1-hydroxycyclohexyl phenyl ketone, 2, 4, 6-trimethyl benzoyl phenyl phosphonic acid ethyl ester, bis 2, 6-difluoro-3-pyrrole phenyl titanocene, phenyl bis(2, 4, 6-trimethylbenzoyl) phosphine oxide, 2-isopropylthioxanthone, 2-hydroxy-2-Methyl-1-phenylacetone, 2-methyl-2-(4-morpholinylphenyl)-1-[4-(methylthio)phenyl]-1-acetone, 1, 7, 7′-Trimethyl-bicyclo(2,2,1)heptane-1,3-dione, tetrafluoroborate methyldiphenylsulfonium salt, 4,4′-dimethyldiphenyliodonium salt fluorophosphate, and combinations thereof; the dark pigment comprises at least one substance having the following structure: ##STR00003## where the range of n is 50-400, and the range of m is 50-400.

2. The dark system photopolymerizable composition according to claim 1, wherein the photopolymerizable prepolymer and/or the photopolymerizable monomer have a polar group, and the polar group is selected from the group consisting of hydroxyl and amino.

3. The dark system photopolymerizable composition according to claim 1, wherein the photopolymerizable prepolymer comprises one or more of polyurethane acrylate, epoxy acrylate, polyester acrylate, and amino acrylic esters.

4. The dark system photopolymerizable composition according to claim 1, wherein the photopolymerizable monomer is selected from the group consisting of monofunctional acrylate monomers, bifunctional acrylate monomers, multifunctional acrylate monomers, ester ring epoxy monomers, oxetane monomers, and combinations thereof.

5. The dark system photopolymerizable composition according to claim 1, wherein the upconversion material is selected from the group consisting of of NaYF4, BaYF5, NaGdF4, LiYF4, NaYbF4, Na3ScF6, YF3, GdOF, and combinations thereof.

6. (canceled)

7. (canceled)

8. (canceled)

9. (canceled)

10. A method of making a dark-colored crosslinked polymer comprising polymerizing the dark-colored photopolymerization composition according to claim 1 under near-infrared light irradiation.

11. The method according to claim 10, wherein the curing depth of the composition is 0.01-30 mm.

12. The method according to claim 10, wherein the wavelength of the near-infrared light is 800-1100 nm; the energy density of the near-infrared light is greater than 1 W/cm.sup.2, less than 20 W/cm.sup.2.

13. The dark system photopolymerizable composition according to claim 1, wherein the photopolymerizable prepolymer comprises one or more of polyurethane acrylate and epoxy acrylate.

14. The dark system photopolymerizable composition according to claim 1, wherein the photopolymerizable monomer is selected from the group consisting of isobornyl acrylate, neopentyl glycol diacrylate, dipentaerythritol hexaacrylate, 1-vinyl-2-pyrrolidone, tetrahydrofuran acrylate, o-phenylphenoxyethyl acrylate, 1,6-hexanediol diacrylate, trimethylolpropane triacrylate, pentaerythritol triacrylate, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexyl formate, and combinations thereof.

15. The dark system photopolymerization composition according to claim 1, wherein the photoinitiator is selected from the group consisting of 2, 4, 6-trimethylbenzoyl diphenyl phosphine oxide, bis 2,6-difluoro-3-pyrrole phenyl titanocene, 4,4′-dimethyl diphenyl iodonium salt fluorophosphate.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] FIG. 1 is a schematic diagram of the photopolymerization of the composition of the invention.

[0027] FIG. 2 shows the curing depth of examples 1-4 and comparison example 5 of the present invention.

[0028] FIG. 3 is the test data curve of embodiment 1-4 and comparison example 5 of the present invention.

[0029] FIG. 4 is the test curve of embodiments 1-4 of the present invention.

DESCRIPTION OF PREFERRED EMBODIMENTS

[0030] The present invention will be described in detail in combination with the drawings and the embodiments.

[0031] As shown in FIG. 1, the photopolymerizable prepolymer, monomer, photoinitiator, melanin and up conversion material are evenly mixed and then put into the test tube. After near-infrared light irradiation, melanin can avoid the absorption of melanin, and can be absorbed by up conversion material and emit ultraviolet or visible light, so as to promote the photoinitiator to decompose and induce the light-emitting polymerization reaction to obtain the final cross-linking product. Melanin synthesis: 180 mg dopamine hydrochloride was dissolved in 90 mL deionized water. At 50° C., 760 μL1 mol/L NaOH solution was added to the above solution. The color of the solution changes to light yellow and gradually turns to dark brown. After aging for 5 hours, the melanin like nanoparticles were recovered by centrifugation at 18000 rpm, washed three times with deionized water and dried. The structure is as follows:

##STR00002##

The range of n is 50-400

Example 1

[0032] the invention relates to a composition for realizing deep photopolymerization of black system

[0033] Polyurethane acrylate 75 phr,

[0034] Trimethylolpropane triacrylate 20 phr,

[0035] Bis (2,6-difluoro-3-pyrrolyl) phenyl titanocene, 3 phr,

[0036] Melanin 0.1 phr,

[0037] Upconversion materials NaYF.sub.4 2 phr.

[0038] The above composition is mixed and evenly added into the test tube, and then placed vertically, the light source with emission wavelength of 980 nm and energy density of 10 W/cm2 is used to irradiate the top of the test tube downward, and a certain length of column is obtained after 5 minutes of curing. When the melanin content is 0.1 phr, the test results are shown in FIG. 2, the length of the column is 29 mm, and the double bond conversion is shown in FIG. 3, which is about 60%. The tensile spline prepared by the composition is tested by mechanics, and the tensile strength is about 27 MPa as shown in FIG. 4.

Example 2

[0039] A composition for realizing deep photopolymerization of black system, the composition contains components and the mass fraction of each component is the same as that in example 1, the difference is that the content of melanin is changed to 0.3 phr, the length of column obtained under the same light conditions is 22 mm as shown in FIG. 2, and the double bond conversion is about 56% as shown in FIG. 3. The tensile spline prepared by the composition is tested by mechanics, and the tensile strength is about 34 MPa as shown in FIG. 4.

Example 3

[0040] A composition for realizing deep photopolymerization of black system, the composition contains components and the mass fraction of each component is the same as that in example 1, the difference is that the content of melanin is changed to 0.5 phr, the length of column obtained under the same light conditions is 17 mm as shown in FIG. 2, and the double bond conversion is about 52% as shown in FIG. 3. The tensile spline prepared by the composition is tested by mechanics, and the tensile strength is about 36 MPa as shown in FIG. 4.

Example 4

[0041] A composition for realizing deep photopolymerization of black system, the composition contains components and the mass fraction of each component is the same as that in example 1, the difference is that the content of melanin is changed to 1 phr, the length of the column obtained under the same light conditions is 9 mm as shown in FIG. 2, and the double bond conversion rate is about 45% as shown in FIG. 3. The tensile spline prepared by the composition is tested by mechanics, and the tensile strength is about 41 MPa as shown in FIG. 4.

[0042] Therefore, with the increase of melanin content, due to the hydrogen bond between melanin and sample, the tensile strength of melanin as a physical cross-linking point increases gradually.

Example 5

[0043] The composition comprises the following components and the mass fraction of each component:

[0044] 75 phr polyurethane acrylate,

[0045] Trimethylolpropane triacrylate 20 phr,

[0046] Bis (2,6-difluoro-3-pyrrolyl) phenyl titanocene, 3 phr,

[0047] Carbon black 0.1 phr,

[0048] Upconversion materials NaYF.sub.4 2 phr.

[0049] The above composition is evenly mixed and added into the test tube. After it is placed vertically, a light source with emission wavelength of 980 nm and energy density of 10 W/cm2 is used to irradiate the top of the test tube downward. After 5 minutes, a certain length of column is obtained by curing. When the carbon black content is 0.1 phr, the test results are shown in FIG. 2. The length of the column is 2 mm, and the double bond conversion is about 40% as shown in FIG. 3.

[0050] Therefore, the barrier ability of carbon black to NIR is higher than that of melanin, which makes NIR difficult to penetrate the sample, the curing depth is limited, and the conversion is lower than that of melanin.

Example 6

[0051] The invention relates to a composition for realizing deep photopolymerization of black system

[0052] Epoxy acrylate 60 phr,

[0053] Pentaerythritol triacrylate 30 phr,

[0054] 2, 4, 6-Trimethylbenzoyldiphenylphosphine oxide, 8 phr,

[0055] Melanin 2 phr,

[0056] Upconversion materials BaYF.sub.5 0.05 phr.

[0057] The composition is evenly mixed, and a 200 micron coating is coated on the surface of the iron plate with a coating coater. The light source with an emission wavelength of 1000 nm and an energy density of 15 W/cm.sup.2 is used to irradiate the coating, and the coating is cured after 1 minute. The conversion rate of the bottom double bond is more than 65%, and the hardness of the coating is 4H.

Example 7

[0058] A composition for realizing deep-layer photopolymerization of a black system, the components contained in the composition and the mass parts of each component are:

[0059] Epoxy resin 50 phr,

[0060] 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexylcarboxylate 40 phr,

[0061] 4,4′-dimethyldiphenyl iodonium salt hexafluorophosphate 3 phr,

[0062] Melanin 5 phr,

[0063] Upconversion materials NaGdF.sub.4 2 phr.

[0064] Mix the above composition uniformly, use a paint film coater to coat a 200-micron coating on the surface of the iron plate, irradiate it with a light source with an emission wavelength of 980 nm and an energy density of 8 W/cm2, and cure after 0.5 minutes. The double bond conversion rate is greater than 60%, and the paint film hardness is 5H.

Example 8

[0065] A composition for realizing deep-layer photopolymerization of a black system, the components contained in the composition and the mass parts of each component are:

[0066] Epoxy resin 70 phr,

[0067] 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexyl 20 phr,

[0068] 4,4′-dimethyldiphenyl iodonium salt hexafluorophosphate 8 phr,

[0069] Melanin 2 phr,

[0070] Upconversion materials LiYF.sub.4 0.05 phr.

[0071] Mix the above composition uniformly, use a paint film coater to coat a 200-micron coating on the surface of the iron plate, irradiate it with a light source with an emission wavelength of 1000 nm and an energy density of 1 W/cm2, and cure after 5 minutes. The double bond conversion of the bottom layer is greater than 60%, and the paint film hardness is 2H.