Preparation of imide oligomers via concurrent reactive extrusion
US-2016215095-A1 · Jul 28, 2016 · US
US10240000B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10240000-B2 |
| Application number | US-201415024838-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 24, 2014 |
| Priority date | Sep 26, 2013 |
| Publication date | Mar 26, 2019 |
| Grant date | Mar 26, 2019 |
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Novel aromatic polyimides are disclosed with sufficient physical properties to be useful in 3D printing.
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What is claimed is: 1. An aromatic polyimide which is a reaction product of (1) 3,4′-oxydianiline (3,4′ ODA); (2) 4,4′-[1,3-phenylenebis(1-methyl-ethylidene)bisaniline (Bisaniline-M); (3) 2,3,3′,4′-biphenyldianhydride (a-BPDA); and (4) phthalic anhydride in a molar ratio of 0.9:0.1:0.975:0.05; wherein the reaction product is in a shape of a filament sufficiently ductile to form a loop of about 64 cm in circumference. 2. The aromatic polyimide of claim 1 in the shape of the filament, wherein the aromatic polyimide has a glass transition temperature of more than 220° C. and ductility to be wound in the shape of the filament of about 2 mm diameter around a spool having a diameter of 8 inches (20.32 cm). 3. The aromatic polyimide of claim 2 in the shape of the filament, wherein the polyimide has a glass transition temperature ranging from about 260 to about 275° C. 4. The aromatic polyimide of claim 2 in the shape of the filament, wherein the polyimide has a glass transition temperature ranging from about 265 to about 270° C. 5. The aromatic polyimide of claim 2 in the shape of the filament, wherein the aromatic polyimide is sufficiently ductile in a length of about 38 cm to be bent upon itself, such that opposing ends of that length of filament can touch each other. 6. The aromatic polyimide of claim 5 , in the shape of the filament wherein the filament has a diameter ranging from about 1.6 to about 2.1 mm. 7. The aromatic polyimide of claim 2 in the shape of the filament, wherein the aromatic polyimide is prepared by solvent-less reactive extrusion. 8. The aromatic polyimide of claim 7 in the shape of the filament, wherein the aromatic polyimide is prepared by concurrent solvent-less reactive extrusion. 9. The aromatic polyimide of claim 1 in the shape of the filament, wherein the polyimide has a glass transition temperature ranging from about 260 to about 275° C. 10. The aromatic polyimide of claim 1 in the shape of the filament, wherein the aromatic polyimide reaction product is sufficiently ductile in a length of about 38 cm to be bent upon itself, such that opposing ends of that length of filament can touch each other. 11. A composite in the shape of the filament comprising the aromatic polyimide of claim 1 . 12. A composite in the shape of the filament comprising the aromatic polyimide of claim 2 . 13. The composite of claim 12 , wherein the composite in the shape of the filament further includes carbon, glass, or synthetic fibers. 14. The composite in the shape of the filament of claim 13 , wherein the composite is further in the form of a 3D printed article.
Preparation · CPC title
in the form of (mono)anhydrid · CPC title
Raw material dosing · CPC title
containing two or more polymers of the same C08L -group · CPC title
characterised by the choice of material · CPC title
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