Cleaning composition
US-2018236717-A1 · Aug 23, 2018 · US
US11850802B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11850802-B2 |
| Application number | US-202117542549-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 6, 2021 |
| Priority date | Aug 14, 2015 |
| Publication date | Dec 26, 2023 |
| Grant date | Dec 26, 2023 |
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Novel support material formulations, characterized as providing a cured support material with improved dissolution rate, while maintaining sufficient mechanical strength, are disclosed. The formulations comprise a water-miscible non-curable polymer, a first water-miscible, curable material and a second, water-miscible material that is selected capable of interfering with intermolecular interactions between polymeric chains formed upon exposing the first water-miscible material to curing energy. Methods of fabricating a three-dimensional object, and a three-dimensional object fabricated thereby are also disclosed.
Opening claim text (preview).
What is claimed is: 1. A support material formulation comprising: a non-curable water-miscible polymer, in an amount that ranges from 30 to 80 weight percent of the total weight of the formulation, said non-curable water-miscible polymer comprising an alkoxylated polyol; a non-curable water-miscible non-polymeric material which comprises 1,2-propanediol; a first water-miscible, curable material in an amount that ranges from 10 to 20 weight percent of the total weight of the formulation; and at least one second water-miscible curable material in an amount that ranges from 5 to 15 weight percent of the total weight of the formulation, wherein said first water-miscible curable material comprises a mono-functional poly(alkylene glycol) acrylate; and wherein said second water-miscible curable material is represented by Formula I: wherein: Ra is selected from H, C(1-4) alkyl and a hydrophilic group; k is an integer ranging from 2 to 10; X is —NRc—, wherein Rc is hydrogen, alkyl, cycloalkyl or aryl; and Y is a hydrogen bond-forming moiety that comprises at least one nitrogen and/or oxygen atom, the formulation being devoid of a multi-functional curable material. 2. The formulation of claim 1 , wherein said second water-miscible curable material is an acrylamide substituted by said hydrogen bond-forming moiety. 3. The formulation of claim 1 , wherein Y is selected from hydroxyl, alkoxy, aryloxy, amine, alkylamine, dialkylamine, carboxylate, hydrazine, carbamate, hydrazine, a nitrogen-containing heteralicyclic, and an oxygen-containing heteralicyclic. 4. The formulation of claim 3 , wherein X is —O—. 5. The formulation of claim 4 , wherein Ra is H, such that the second curable material is an acrylate. 6. The formulation of claim 1 , wherein Ra is H, such that the second curable material is an acrylamide. 7. The formulation of claim 1 , wherein said water-miscible polymer comprises said alkoxylated polyol and a polyethylene glycol. 8. The formulation of claim 1 , wherein a concentration of said second water-miscible curable material ranges from 5 to 10 weight percent of the total weight of the formulation. 9. The formulation of claim 1 , further comprising an initiator, a surface active agent and/or an inhibitor. 10. The formulation of claim 1 , wherein each of said first and second water-miscible curable materials is a UV-curable material. 11. The formulation of claim 1 , wherein a cured support material formed upon exposing the formulation to a curing energy is dissolvable in an alkaline solution. 12. The formulation of claim 11 , wherein a dissolution time of a cured support material when immersed in said alkaline solution is at least 2-folds, or at least 4-folds, shorter than a dissolution time of a cured support material made of a comparable support material formulation that is absent said second water-miscible curable material. 13. The formulation of claim 11 , wherein a dissolution time of a 16-grams cube made of said cured support material and immersed in 800 ml of said alkaline solution is less than 2 hours. 14. The formulation of claim 1 , wherein a cured support material formed upon exposing the formulation to a curing energy is characterized by a mechanical strength that is lower than a mechanical strength of a cured support material made of a comparable support material formulation that is absent said second water-miscible curable material and comprises substantially the same total concentration of curable materials as the formulation, by no more than 50% or by no more than 40%, or by no more than 30%.
Structures for supporting 3D objects during manufacture and intended to be sacrificed after completion thereof · CPC title
using individual droplets, e.g. from jetting heads · CPC title
Cleaning · CPC title
Processes of additive manufacturing · CPC title
Post-treatment, e.g. curing, coating or polishing · CPC title
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