A DIRECT INK WRITING THREE-DIMENSIONAL PRINTING METHOD BASED ON NEAR-INFRARED PHOTOPOLYMERIZATION

Abstract

The invention relates to an ink based on near-infrared light polymerization. The method and technology of direct writing three-dimensional printing belong to the field of material processing technology area. The method is: direct writing nozzles move in three-dimensional space or stationery, the ink is squeezed out of the direct writing nozzle, receiving the near-infrared light irradiation, after curing, complete the three-dimensional object forming and curing. The solidifying time t does not exceed the ratio of near-infrared light diameter d.sub.1 and the ink extrusion speed vi, that is, t≤d.sub.1/v.sub.i. Since near-infrared light has a better medium mass penetration, can penetrate the structure during molding to promote both internal and external to a higher degree of curing, so as to achieve cross-scale structure 3D printing, and the method provided by the present invention accurately controls solidifying process of the ink and therefore achieve the DIW array 3D structure real-time curing.

Claims

1. A direct ink writing three-dimensional printing method based on near-infrared photopolymerization, wherein the method is as follows: the direct writing nozzle moves or stands still in a three-dimensional space, and the ink is extruded out of the direct writing nozzle, under the irradiation of near-infrared light, the 3D printed object is solidified after photocuring, and the curing time t does not exceed the ratio of the near-infrared light diameter (d.sub.1) to the slurry extrusion speed (v.sub.i), that is, t≤d.sub.1/v.sub.i; the rheological properties of the ink should satisfy; the elastic modulus G′ is 0.5-5 times the loss modulus G″, that is, 0.5G″≤G′≤5G′; the composition of the ink is as follows: 0-80 wt. % photopolymerizable resin, 0-80 wt. % photopolymerizable monomer, 0.5-6 wt. % photoinitiator, 0.5-5 wt. % upconversion material, 0-30 wt. % thixotropic agent, 2-30 wt. % fillers; the moving speed of the direct writing nozzle is 0 to 5.0 mm/s.

2. The method according to claim 1, wherein the diameter of the direct writing nozzle is in the range of 0.1 μm to 10 cm.

3. (canceled)

4. (canceled)

5. The method according to claim 1, wherein the force for ink-extruding is pressure, and the pressure does not exceed 800 kPa.

6. The method according to claim 1, wherein the near-infrared laser is a light beam or light spot, and the light spot or light beam is located within 1 cm of the direct writing nozzle.

7. The method according to claim 1, wherein the power of the near-infrared laser is 0-50 W, and the wavelength range is 700-2000 nm.

8. The method according to claim 1, wherein the photopolymerizable resin includes a resin containing an acrylate double bond, a resin containing a vinyl ether double bond, and a resin containing an epoxy group; the photopolymerizable monomer include one or more of the following monomers: monofunctional acrylate monomers, difunctional acrylate monomers, multifunctional acrylate monomers, vinyl ether monomers, ester ring epoxy monomers, oxetane monomers. the photoinitiator include one or more of following initiators: 2,4,6-trimethyl benzoyl 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 methyl diphenyl sulfonium salt; 4,4′-dimethyl diphenyl iodonium salt hexafluorophosphate; ferrocene hexafluorophosphate; the up-conversion material includes one or more of NaYF4, BaYF5, NaGdF4, LiYF4, NaYbF4, Na3ScF6, YF3, and GdOF; the thixotropic agent includes fumed silica; the filler includes one or more of barium sulfate, titanium dioxide, silicon dioxide, and talc.

9. The method according to claim 1, wherein the ink contains pigments.

10. (canceled)

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0028] FIG. 1 is a device for DIW 3D printing based on near-infrared photopolymerization, in which 1 is a support table; 2 is a near-infrared light emitting structure; 3 is a controller; 4 is a direct writing nozzle; 5 is an ink storage tank; 6 The printed three-dimensional object.

[0029] FIG. 2 is an ultra-widefield microscope image of the conversion rate and morphology of samples obtained by using different diameters;

[0030] FIG. 3 is a contrast image of a sample obtained without near-infrared real-time curing and a sample obtained with near-infrared real-time curing

[0031] FIG. 4 is a microscope image of the conversion rate and morphology of the sample printed with inks mixed with different pigments

[0032] FIG. 5 is the ultraviolet-visible light absorption spectra of the initiator Iragacure 784 and four pigments used in the examples

[0033] FIGS. 6a and b are respectively a sample diagram and a cross-sectional view of a sample with different colors inside and outside obtained by using two color inks for coaxial printing in Example 4.

[0034] FIGS. 7a and b are two different 3D printed bodies with suspended structures obtained in Example 5 respectively.

DESCRIPTION OF PREFERRED EMBODIMENTS

Example 1

[0035] FIG. 1 is a near-infrared light polymerized DIW 3D printing device, which is composed of a support table 1, a near-infrared light emitting structure 2, a controller 3, a direct writing nozzle 4, and an ink storage tank 5.

[0036] The support table 1 is used to support three-dimensional objects 6; the near-infrared light emitting structure 2 is located above the support table 1, and is fixedly connected to the controller 3. The controller 3 drives the near-infrared light emitting structure 2 to move or stand still; the direct writing nozzle 4 is located Above the supporting table 1, the direct writing nozzle 4 and the ink storage tank 5 are hermetically connected, the direct writing nozzle 4 and the ink storage tank 5 are fixedly connected with the controller 3, and the controller 3 drives the direct writing nozzle 4 and the ink storage tank 5 to move or stop.

[0037] Raw material 1.0 wt. % initiator (Irgacure 784), 1.0 wt. % NaYF4 up-conversion nanoparticles, 13.0 wt. % thixotropic agent (Aerosil, Evonik TS100), 42.5 wt. % epoxy acrylate resin and 42.5 wt. % monomer. After weighing the trimethylolpropane acrylate (TMPTA), it is fully mixed in the mixed defoamer to obtain the ink (the elastic modulus G′ is 0.53 kPa, and the loss modulus G″ is 0.28 kPa). Fill the ink into the ink storage tank, control the extrusion pressure to 50 kPA, the ink is extruded through the direct writing nozzle (0.21, 0.41, 0.80, 1.55, 2.50, 4.00 mm), and the direct writing nozzle is made in the horizontal plane through the controller. In reciprocating motion, the laser emitting structure and the direct writing nozzle are relatively static, and the beam is located 2 mm directly below the direct writing nozzle. The laser emitting structure emits a light beam with a wavelength of 980 nm, the laser power is 3.5 W, and the printing speed is controlled at 1.0 mm/s. Lines with different line widths can be obtained, as shown in FIG. 2. The characteristic absorption peak changes are measured by total reflection Fourier transform infrared spectroscopy. No matter the line diameter is widened (0.41-4.00 mm), the conversion rate does not fluctuate significantly, at about 50%, which proves that the near-infrared penetration can achieve uniform curing.

Example 2

[0038] Real-time curing using near-infrared light: using the same process parameters, direct writing printing equipment and working parameters of the ink in Example 1, only 0.41 mm nozzles are used for grid printing (first control the direct writing nozzles to reciprocate in the horizontal plane, and then control the direct writing nozzle lifted and changes the original direction of movement to continue reciprocating motion) to obtain a 3D printed object as shown in the right of FIG. 3.

[0039] For curing using near-infrared light after printing: using the same ink process parameters, direct writing printing equipment and working parameters mentioned above, using 0.41 mm nozzles for grid printing, the ink moves with the direct writing nozzles and is extruded to obtain the shape, After the extrusion is finished, the near-infrared light is used for curing to obtain a 3D printed object as shown in the left of FIG. 3.

[0040] A comparison is made between using near-infrared light to cure after printing and using near-infrared light to cure in real time, as shown in FIG. 2. The lines of the post-cured sample collapsed, while the lines of the real-time cured sample remained better and the structure was regular.

Example 3

[0041] The working setup of the near-infrared photopolymerized ink direct-write 3D printing equipment is the same as in Example 1. The 1.0% wt initiator (Irgacure 784), 1.0 wt % NaYF4:Yb, Tm up-conversion nanoparticles, 0.5 wt. % colorant (red , Yellow, blue, white), 12.5 wt. % thixotropic agent (aerosol, Evonik TS100), 42.5 wt. % epoxy acrylate resin and 42.5 wt. % monomer trimethylolpropane acrylate (TMPTA) after weighing In the mixed defoaming machine, the ink is obtained by fully mixing (the elastic modulus G′ is 0.49 kPa, and the loss modulus G″ is 0.25 kPa). Fill the ink into the printer, control the extrusion pressure to 50 kPA, use a 1.55 mm direct writing nozzle, the laser power is 3.5 W, and the printing speed is controlled to 1.0 mm/s. Lines of different colors can be obtained, and the result is shown in FIG. 4. As shown in FIG. 5, according to the ultraviolet-visible light absorption spectrum, the absorption band (300-500 nm) of the initiator used overlaps with the absorption peak of the color paste, and there is a competitive relationship in the process of absorbing and using the energy of the light source. If ultraviolet-blue light is used Printing curing is difficult to achieve curing. The characteristic absorption peak changes of samples after NIR curing were measured by total reflection Fourier transform infrared spectroscopy. The phase conversion rate of different colors did not fluctuate significantly, at about 40%, which proved that the color samples can be cured by using near-infrared penetration.

Example 4

[0042] Use coaxial nozzles (outside 1.3 mm, inside 0.5 mm) for simultaneous dual-color extrusion of the color paste in Example 3 under the same process: use coaxial nozzles (outside 1.3 mm, inside 0.5 mm) as direct writing nozzles, At the same time, the two-color inks are filled and connected to the inner and outer flow channels of the coaxial nozzle, and they are extruded under the force and are irradiated by the near-infrared to realize curing to obtain lines with two colors inside and outside. It is proved that it is possible to realize multi-color/multi-material by using near-infrared penetration, and the result is shown in FIG. 6.

Example 5

[0043] Under the printing parameters in Example 3, by simultaneously raising the direct writing nozzle and the near-infrared light spot, the ink is gradually extruded from the substrate into the suspended air and solidified, so that 3D printing of a self-supporting suspended structure can be realized. Compared with traditional 3D printing methods, such as thermally cured ink direct writing, techniques such as stereo lithography need to add additional support to the suspended structure and cut after printing. The method utilizes the penetrability and controllability of near-infrared curing to promote the ink to reach the gel point quickly and uniformly to realize the self-supporting ability.