COMPOSITION OF PHOTOPOLYMERIZABLE RESINS AND METHOD TO PRODUCE AN ARTICLE USING THIS COMPOSITION

Abstract

There are described compositions of photopolymerizable resins containing functional (meth)acrylic groups and one or more radical polymerization photoinitiators, stereolithographic methods of producing articles using these resins and articles thus obtained.

Claims

1-10. (canceled)

11. A composition of photopolymerizable resins comprising: (A) derivatives of diurethane dimethacrylates having the following formula: ##STR00010## wherein R and R′ are the same or different, and are selected from H and methyl, and/or its oligomers with a molecular weight up to 6000 g/mol; (B) one or more of the following (meth)acrylic monomers: ##STR00011## ##STR00012## ##STR00013## (C) one or more radical polymerization photoinitiators for said monomers and/or oligomers.

12. The composition of claim 11, comprising a component (D) consisting of one or more additives chosen from the group consisting of organic and inorganic dyes and UV absorbers for the control of the printing resolution with high absorbance at the typical wavelengths of the radiant sources.

13. The composition of claim 11, wherein said monomers and/or oligomers have a viscosity at room temperature between 100 and 1000 mPa.Math.s.

14. The composition of claim 11, wherein said component (A) is present in an amount from 60 to 90% by mass.

15. The composition of claim 11, wherein said component (B) is present in an amount from 10 to 40% by mass.

16. The composition of claim 11, wherein said component (C) is present in an amount from 0.5 to 3% by mass.

17. The composition of claim 12, wherein said component (D) is present in an amount from 0.005 to 0.05% by mass.

18. A method to form a three-dimensional article, the method comprising: (1) depositing on a surface a first thin layer of the composition of photopolymerizable resins according to claim 1; (2) exposing said thin layer to a photopolymerizing radiation of sufficient intensity to cause the resins of said thin layer to polymerize; (3) depositing a second thin layer of said composition of photopolymerizable resins on said first thin layer previously exposed to said photopolymerizing radiation; (4) exposing said second thin layer to said photopolymerizing radiation of sufficient intensity to cause the resins of said second thin layer to polymerize and to cause adhesion to said first thin layer; (5) repeating steps (3) and (4) a sufficient number of times to manufacture said article; and (6) subjecting the article obtained to a post-curing treatment comprising irradiation with a radiation of a wavelength between 300 and 450 nm, at a temperature between 50 and 100° C. and for a time between 30 and 90 minutes.

19. The method of claim 18, wherein: in said step (1) said composition of photopolymerizable resins is poured into a printing tank with a transparent bottom, creating said first thin layer on the bottom of said tank; in said step (2) a growth platform is lowered to the bottom of said tank and said first layer is irradiated by a suitable source positioned underneath the tank, in order to solidify said resins; in said step (3) said growth platform, on which the solidified part of said photopolymerizable resins remains attached, is lifted and another part of photopolymerizable resin is poured on the bottom of said tank with the formation of a second thin layer of liquid resin on the transparent bottom of said tank; in said step (4) said growth platform is lowered to the bottom of said tank and said second layer is irradiated by said source positioned underneath the tank, in order to solidify said second layer of resins on said first layer of resins; in said step (5) the process is repeated for a sufficient number of layers to produce said three-dimensional article; and in said step (6) said article undergoes said post-curing treatment.

20. An HTM resin article obtained by photopolymerization of said composition of photopolymerizable resins according to claim 1, said article having a Shore D hardness between 50 and 90 measured according to ISO 868.

Description

DESCRIPTION OF THE INVENTION

[0031] The term “liquid” used in the present description is meant as “liquid at room temperature”, which is a temperature between 5° C. and 30° C.

[0032] The term “(meth)acrylate” as used in the present description designates both acrylates and methacrylates.

[0033] The new composition according to the invention is a composition of photopolymerizable resins comprising: [0034] (A) Derivatives of diurethane dimethacrylates having the following formula:

##STR00005## [0035] wherein R and R′ are the same or different, and are selected from H and methyl, [0036] and/or its oligomers with a molecular weight up to 6000 g/mol; and [0037] (B) One or more of the following (meth)acrylic monomers:

##STR00006##

##STR00007##

##STR00008## [0038] (C) One or more radical polymerization photoinitiators for said monomers and/or oligomers.

[0039] A preferred photoinitiator is the phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide having the following formula (IV):

##STR00009##

[0040] Preferably, the composition also includes a component (D) consisting of one or more additives chosen from the group consisting of organic and inorganic dyes and UV absorbers for the control of the printing resolution with high absorbance at the typical wavelengths of the radiant sources.

[0041] The blend of two or more monomers and/or oligomers (A) and (B) makes it possible to obtain a suitable compromise between viscosity of the liquid blend and final crosslinking density. In fact, the viscosity is sufficiently low to allow correct processing/printing. The crosslinking density, expressed as number of crosslinking points per unit of mass, is high and allows high thermal-mechanical (HTM) properties to be obtained.

[0042] Preferably, the monomers and/or oligomers (A) and (B) have a viscosity at room temperature between 100 and 1000 mPa.Math.s.

[0043] The component (A) is preferably present between 60 and 90% by mass.

[0044] The component (B) is preferably present between 10 and 40% by mass.

[0045] The component (C) is preferably present between 0.5 and 3% by mass.

[0046] The component (D) is preferably present between 0.005 and 0.05% by mass.

[0047] The functional groups reactive at the photopolymerization reactions of the oligomers are of acrylic and/or methacrylic type.

[0048] In an embodiment, the component (A) is the reactive oligomer composed of an aliphatic urethane methacrylate resin with two acrylic functions and a viscosity of around 7000 mPa.Math.s, such as the product with the trade name Allnex Ebecryl° 4859. In an embodiment, the component (B) is the reactive oligomer trimethylolpropane triacrylate (TMPTA).

[0049] In an embodiment, the component (C) is the photoinitiator bis-acylphosphine oxide, such as the product with the trade name IGMResins Omnirad® 819.

[0050] In an embodiment, the component (D) is the dye2-phenyl-4-[(1-phenyl-1,5-dihydro-3-methyl-5-oxy-4H-pyrazol-4-ylidene)methyl]-2,4-dihydro-5-methyl-3H-pyrazol- 3-one, such as the product with the trade name Oracet® Yellow 130 by BASF AG.

[0051] The reactive oligomers containing acrylic or methacrylic groups undergo a radical photopolymerization chain reaction. The start of the polymerization/crosslinking reaction takes place following dissociation of the photoinitiators with formation of free radicals.

[0052] Dissociation of the photoinitiator is caused by irradiation of the system with an electromagnetic radiation of suitable frequency (wavelength). The wavelength of the radiation is variable from around 300 nm to 450 nm as a function of the VAT photopolymerization printer used.

[0053] The liquid compositions are obtained by mechanical blending of the various components at room temperature. To facilitate the dissolution process of the solid components such as the photoinitiator and the dye, these are previously dissolved in the least viscous reactive monomer/oligomer. After obtaining a homogeneous solution, the reactive oligomer with the highest viscosity is added and mixed.

[0054] The liquid composition can be used in an additive manufacturing stereolithography method, to form a three-dimensional article comprising the following steps: [0055] (1) depositing a first thin layer of the composition of photopolymerizable resins on a surface; [0056] (2) exposing said thin layer to a photopolymerizing radiation of sufficient intensity to cause the resins of said thin layer to polymerize; [0057] (3) depositing a second thin layer of said composition of photopolymerizable resins on said first thin layer previously exposed to said photopolymerizing radiation; [0058] (4) exposing said second thin layer to said photopolymerizing radiation of sufficient intensity to cause the resins of said second thin layer to polymerize and to cause adhesion to said first thin layer; and [0059] (5) repeating steps (3) and (4) a sufficient number of times to manufacture said article; and [0060] (6) subjecting the article obtained to a post-curing treatment comprising irradiation with a radiation of a wavelength between 300 and 450 nm, at a temperature between 50 and 100° C. and for a time between 30 and 90 minutes.

[0061] According to an embodiment, the additive manufacturing method is a bottom-up stereolithography method, wherein: [0062] the liquid resin is poured into a printing tank with a transparent bottom; [0063] a growth platform is lowered creating a first thin layer of liquid resin on the transparent bottom of the tank; [0064] the first layer is selectively cross-linked/solidified following irradiation coming from a suitable source, such as a laser point source or LCD, positioned under the tank; [0065] the growth platform, on which the solidified part remains attached, is lifted to allow the creation of a new thin layer of liquid resin on the transparent bottom of the tank; [0066] the process is repeated for a sufficient number of layers to produce the three-dimensional object as per digital project.

[0067] The crosslinking/solidification chemical reaction is not generally completed during the printing step, which thus produces a “green” article. In particular, due to chemical-physical vitrification phenomena, chemical conversion remains below 100%. To complete the chemical reaction and thus develop the maximum crosslinking density value and optimization of the thermo-mechanical properties of the end product, a post-curing step is required, i.e., a heat and/or irradiation treatment adapted to promote completion of the chemical reactions.

[0068] An example of post-curing treatment consists of exposure to UV irradiation (wavelength of 405 nm), at the temperature of around 70° C. and for a time of 1 hour. The examples set forth below illustrate some embodiments of the invention and are provided by way of non-limiting example.

EXAMPLES

[0069] The following examples show the amount of each component (A), (B), (C) and (D) in the photopolymerizable resins according to the invention.

Example 1

[0070]

TABLE-US-00001 Concen- tration (% Components mass) Reactive oligomer Allnex Ebecryl ® 4859 (Component A) 79.0 Reactive oligomer trimethylolpropane triacrylate (Component B) 18.5 Photoinitiator bis-acylphosphine oxide (Component C)  2.0 Dye 2-phenyl-4-[(1-phenyl-1,5-dihydro-3-methyl-5-oxy-4H-  0.5 pyrazol-4-ylidene)methyl]-2,4-dihydro-5-methyl-3H-pyrazol-3- one (Component D)

Example 2

[0071]

TABLE-US-00002 Concen- tration (% Components mass) Reactive oligomer Allnex Ebecryl ® 4859 (Component A) 59.0 Reactive oligomer trimethylolpropane triacrylate (Component B) 38.5 Photoinitiator bis-acylphosphine oxide (Component C)  2.0 Dye 2-phenyl-4-[(1-phenyl-1,5-dihydro-3-methyl-5-oxy-4H-  0.5 pyrazol-4-ylidene)methyl]-2,4-dihydro-5-methyl-3H-pyrazol-3- one (Component D)

Example 3

[0072]

TABLE-US-00003 Concen- tration (% Components mass) Reactive oligomer Allnex Ebecryl ® 4859 (Component A) 39.0 Reactive oligomer trimethylolpropane triacrylate (Component B) 58.5 Photoinitiator bis-acylphosphine oxide (Component C)  2.0 Dye 2-phenyl-4-[(1-phenyl-1,5-dihydro-3-methyl-5-oxy-4H-  0.5 pyrazol-4-ylidene)methyl]-2,4-dihydro-5-methyl-3H-pyrazol-3- one (Component D)

[0073] Table 1 below gives some properties of the compositions of Examples 1-3.

TABLE-US-00004 TABLE 1 Conservative Conservative Glass transition Viscosity modulus.sup.1,2 modulus.sup.1,2 at temperature.sup.1,3 Example (mPa s) at 25° C. (MPa) 100° C. (MPa) (° C.) 1 700-800 2700 850 150 2 600-700 2900 950 110 3 400-500 2400 790  60 .sup.1After post-curing: 1 hour at the temperature of 70° C. and with UV irradiation .sup.2Determined by dynamic-mechanical analysis at the frequency of 1 Hz, according to ISO 6721 .sup.3Determined by dynamic-mechanical analysis at the frequency of 1 Hz and at the loss factor peak (loss factor, tan ™ ), according to ISO 6721

[0074] The material obtained following 3D printing with the HTM resins has a hard and vitreous consistency with Shore D hardness between 50 and 90, measured according to ISO 868.

[0075] Application of the material obtained following 3D printing from HTM resins relates to the production of articles intended for any purpose which requires the use of a plastic material with features of stiffness at high temperatures (up to 250° C.). A specific example of the use of this material is in the production of mould inserts to be used in the injection moulding of thermoplastic polymers.

[0076] Compared to the PEG resins described in the Italian patent application No. 102018000008679 cited previously, the articles obtained from HTM resins according to the present invention show the main differences indicated in Table 2:

TABLE-US-00005 TABLE 2 Post- Type Elastic curing Use at high of Chemical modulus treat- temperature resin structure Hardness (MPa) ment (>150° C.) PEG Poly(ethylene glycol) 20-80 0.1-10  No No Base diacrylate Shore A HTM Esters of acrylic or 50-90 1000-5000 Yes Yes methacrylic acid, Shore D acrylic or methacrylic urethanes

[0077] The advantage of the HTM resins according to the present invention in allowing the production of three-dimensional articles that are easy to design and of high quality with a highly reliable process must also be highlighted.