INK COMPOSITION FOR POWDER BED AND INKJET HEAD 3D PRINTING
20170066936 ยท 2017-03-09
Assignee
Inventors
- Heonju Lee (Seoul, KR)
- Myoungwoon Moon (Seoul, KR)
- Wonjin Jo (Seoul, KR)
- Sangsoo Han (Seoul, KR)
- Haeshin Lee (Seoul, KR)
- Intaek Song (Seoul, KR)
Cpc classification
C09D11/38
CHEMISTRY; METALLURGY
B29K2105/0032
PERFORMING OPERATIONS; TRANSPORTING
B33Y70/00
PERFORMING OPERATIONS; TRANSPORTING
B29K2105/251
PERFORMING OPERATIONS; TRANSPORTING
C09D11/03
CHEMISTRY; METALLURGY
B29K2105/0097
PERFORMING OPERATIONS; TRANSPORTING
B29K2105/0044
PERFORMING OPERATIONS; TRANSPORTING
B29C71/0009
PERFORMING OPERATIONS; TRANSPORTING
C09D11/101
CHEMISTRY; METALLURGY
International classification
C09D11/03
CHEMISTRY; METALLURGY
B33Y70/00
PERFORMING OPERATIONS; TRANSPORTING
B29C71/00
PERFORMING OPERATIONS; TRANSPORTING
B33Y30/00
PERFORMING OPERATIONS; TRANSPORTING
B29C67/00
PERFORMING OPERATIONS; TRANSPORTING
B33Y40/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
The present invention relates to an ink composition containing a multifunctional adhesive suitable for a three-dimensional (3D) printer and the use thereof. The multifunctional adhesive of the present invention contains a compound with a catechol group and exhibits excellent adhesion to various materials (e.g. dry plaster powders, polymers, metals, ceramics, and composite materials). The use of the ink composition of the present invention containing the multifunctional adhesive enables the processing of various functional materials that were difficult to fabricate into a 3D structure. Therefore, it is highly likely that the ink composition of the present invention can effectively create a market for functional materials for a 3D printer and find new areas of application (e.g. automotive, medical, fashion, aviation/aerospace, construction, consumer electronics, entertainment, etc.).
Claims
1. An ink composition for three-dimensional (3D) printing comprising an adhesive, a solvent, a stabilizer, and a viscosity controlling agent, wherein the adhesive is a compound containing a catechol group.
2. The ink composition of claim 1, wherein the ink composition contains the adhesive at 10 to 30% by volume, the solvent at 40 to 60% by volume, the stabilizer at 5 to 10% by volume, and the viscosity controlling agent at 20 to 40% by volume.
3. The ink composition of claim 1, wherein the ink composition has an Ohnesorge number (Oh) ranging from 0.1 to 1.0.
4. The ink composition of claim 1, wherein the adhesive is a polydopamine, chitosan-catechol, hyaluronic acid-catechol, or alginate-catechol.
5. The ink composition of claim 1, wherein the solvent is an alcohol-based solvent.
6. The ink composition of claim 1, wherein the stabilizer is anhydrous 2-ethylhexyl acrylate (2-EHA) or 2-methoxyethanol (2-ME).
7. The ink composition of claim 1, wherein the viscosity controlling agent is ethylhexanoic acid or 1,2-propanediol.
8. The ink composition of claim 1, wherein the ink composition further comprises an oxidizing agent or a dye.
9. The ink composition of claim 8, wherein the oxidizing agent is piperidine.
10. The ink composition of claim 8, wherein the dye is an organic or inorganic dye listed in the Colour Index International.
11. A method of producing a structure using three-dimensional (3D) printing, the method comprising: (a) preparing the ink composition of claim 1; and (b) producing the structure (part) by introducing the composition into a 3D printer and continuously supplying a powder material.
12. The method of claim 11, further comprising: (c) a post-processing treatment.
13. The method of claim 12, wherein the post-processing treatment (c) comprises any one or both of polishing the structure with a post-processing material (c-1) and finishing the structure with a finish type (c-2).
14. The method of claim 13, wherein the post-processing material is a resin, an epoxy resin, an acrylic resin, Dragon Skin, or a fiber-reinforced plastic (FRP).
15. The method of claim 13, wherein the finish type is a resin finish, a sand-blasted finish, a resin dye finish, or an integral color finish.
16. A three-dimensional (3D) printing system using the ink composition of claim 1.
17. The 3D printing system of claim 16, wherein the 3D printing system is a powder bed and inkjet head 3D printing system.
Description
DESCRIPTION OF DRAWINGS
[0049]
[0050]
[0051]
[0052]
MODES OF THE INVENTION
[0053] Hereinafter, the present invention will be described in further detail with reference to exemplary embodiments. The exemplary embodiments are only for describing the present invention more specifically, and it will be clear to those skilled in the art that the gist and scope of the present invention are not limited to those exemplary embodiments
EXAMPLES
Example 1
Analysis of Polydopamine Adhesive Properties
[0054]
[0055] In the above equation, is the viscosity coefficient, is the surface energy, is the density, L is the characteristic length scale, Re is the Reynolds number, and We is the Weber number [B. Derby and N. Reis, Inkjet Printing of Highly Loaded Particulate Suspensions, MRS Bulletin, pp. 815-818 (2003)]. The Ohnesorge number of each ingredient can be calculated using the above equation.
[0056] The conventional powder bed and inkjet head 3D printing system took advantage of binding between a material in a powder form 4 and a special liquid adhesive 7 as a result of a particular reaction (i.e. a self-hydration reaction) therebetween (
[0057] To study if the polydopamine can have an adhesion property that is equal, similar, or superior to that of a conventional binder, the present inventors examined the roles of a binder and a polydopamine in the adhesion between a powder and TiO.sub.2 (2.5 mg). As shown in
Example 2
Analysis of Adhesion Of Polydopamine Adhesive
[0058] To study the functionality of a polydopamine as a general-purpose adhesive in more detail, the ingredients were mixed in the composition shown in the following Table 1 for 24 hours at room temperature. The precipitates obtained by the centrifugation of the liquid mixture were washed with ethanol 5 times. The mixture that had been washed was then centrifuged at 1,200 rpm and 2,000 rpm, and the precipitation status was observed.
TABLE-US-00001 TABLE 1 Sample number Composition Mixing condition 1 (Ethanol + TiO.sub.2 + powder + Four ingredients are mixed dopamine) together 2 (Ethanol + powder + dopamine) + TiO.sub.2 is added after binding TiO.sub.2 dopamine to the powder 3 (Ethanol + TiO.sub.2 + powder + An oxidizing agent (piper- dopamine + piperidine) idine) is added to Sample 1 4 (Ethanol + powder + dopamine + TiO.sub.2 is added to Sample 2 piperidine) + TiO.sub.2 5 (Ethanol + TiO.sub.2 + powder) Ingredients are mixed in an absence of the dopamine adhesive
[0059] Excellent Adhesion of Polydopamine
[0060] More specifically, when the precipitation by centrifugation was performed at 1,200 rpm, the added dopamine (2 mg/ml; dissolved in ethanol) induced the stable adhesion of TiO.sub.2 (2.5 mg) to the powder (250 mg), leading to the formation of distinct precipitates. In contrast, in an absence of the dopamine adhesive, TiO.sub.2 did not adhere to the powder, and precipitates were not produced during centrifugation at 1,200 rpm (
[0061] In addition, the ingredients in parentheses in Samples 1 to 4 of Table 1 were first mixed and then were dried. The dried mixture was again added to ethanol and then was subjected to centrifugation. When the centrifugation was performed at 2,000 rpm, all of Samples 1 to 4 were well precipitated and could be separated with ease. Moreover, when the addition of TiO.sub.2 was performed after the drying of a mixture of other ingredients (i.e. Samples 2 and 4), the adhesion of TiO.sub.2 occurred successfully and precipitates were observed (
Example 3
3D Printing Using Polydopamine Adhesive
[0062] To demonstrate the effectiveness of a polydopamine in 3D printing, the present inventors performed 3D printing in both absence (
[0063] Detailed descriptions of specific parts of the context of the present invention have been provided above. However, it will be clear to those skilled in the art that such specific descriptions are merely exemplary and do not limit the scope of the present invention. Therefore, the actual scope of the present invention is determined by the appended claims and their equivalents.