Material preparation and feeding system of a construction 3d printer
US-2024300177-A1 · Sep 12, 2024 · US
US10836117B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10836117-B2 |
| Application number | US-201815977428-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 11, 2018 |
| Priority date | Apr 29, 2008 |
| Publication date | Nov 17, 2020 |
| Grant date | Nov 17, 2020 |
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The present invention relates to a method for reducing the crystallization temperature an the melting temperature of a polyamide powder resulting from the polymerization of at least one predominant monomer, in which the reduction in the crystallization temperature is greater than the reduction in the melting temperature, said method comprising a step of polymerization of said at least one predominant monomer with at least one different minor comonomer polymerized according to the same polymerization process as said at least one predominant monomer, said at least one minor comonomer being chosen from aminocarboxylic acids, diamine/diacid pairs, lactams and/or lactones, and said at least one minor comonomer representing from 0.1% to 20% by weight of the total blend of said monomers(s) and comonomer(s), preferably from 0.5% to 15% by weight of said total blend, preferably from 1% to 10% by weight of said total blend.
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The invention claimed is: 1. A process for reducing the crystallization temperature and the melting temperature of a polyamide derived from the polymerization of only one major monomer, said process comprising: polymerization of said only one major monomer with only one different minor comonomer polymerized according to the same polymerization process as said only one major monomer, said only one minor comonomer selected from the group consisting of 11-aminoundecanoic acid, lauryllactam, caprolactam, caprolactone, and a diamine-diacid selected from the group consisting of: 6.6, 6.10, 6.11, 6.12, 6.14, 6.18, 10.10, 10.12, 10.14, 10.18 and 10.T, T being terephthalic acid, minor comonomer representing from 1% to 7% by mass of the total blend of said monomer and comonomer, such that the reduction in the crystallization temperature is greater than the reduction in the melting temperature, relative to the crystallization temperature and the melting temperature of the polyamide obtained from the polymerization of said major monomer, wherein the polyamide obtained from the polymerization of said major monomer is a powder with a particles size of 10 μm to 350 μm, wherein the major monomer is selected from the group consisting of 11-aminoundecanoic acid, lactam 12, and decanediamine-sebacic acid couple (10.10), and wherein the change in the crystallization temperature is at least 5° C. 2. The process as claimed in claim 1 , in which said polymerization is an anionic polymerization. 3. The process as claimed in claim 1 , in which said polymerization is a hydrolytic polycondensation. 4. The process as claimed in claim 1 , further comprising, after said polymerization, at least one of the following process selected from the group consisting of dissolution, precipitation, extrusion, atomization, spraying, cold nebulization, hot nebulization, milling, cryogenic milling, screening, viscosity raising, and combinations thereof, is conducted. 5. A copolyamide or copolyesteramide powder obtained from the polymerization of only two different monomers polymerized according to the same polymerization process, one of the monomers being minor and selected from the group consisting of 11-aminoundecanoic acid, lauryllactam, caprolactam, caprolactone, and a diamine-diacid selected from the group consisting of 6.6, 6.10, 6.11, 6.12, 6.14, 6.18, 10.10, 10.12, 10.14, 10.18 and 10.T, T being terephthalic acid, said one minor monomer representing from 1% to 7% by mass of the total blend of said monomer(s) representing from 1 to 7% by mass of the total blend of said monomer(s), and wherein the copolyamide or copolyesteramide powder has particles size of 10 um to 350 um and wherein the change in the crystallization temperature is at least 5° C. 6. The powder claimed in claim 5 , comprising an 11-aminoundecanoic acid major monomer and a minor monomer selected from the group consisting of hexamethylenediamine-adipic acid couple (6.6), lauryllactam, caprolactam, and caprolactone. 7. The powder as claimed in claim 5 , comprising a lauryllactam major monomer and a minor monomer selected from the group consisting of caprolactam, caprolactone, hexamethylenediamine-adipic acid couple (6.6) and mixtures thereof. 8. A process for manufacturing a polyamide article comprising melt-induced powder aggregation using electromagnetic radiation of a polyamide powder obtained from the polymerization of two different monomers polymerized according to the same polymerization process, one of the monomers being minor and selected from the group consisting of 11-aminoundecanoic acid, lauryllactam, caprolactam, caprolactone, and a diamine-diacid couple selected from the group consisting of 6.6, 6.10, 6.11, 6.12, 6.14, 6.18, 10.10, 10.12, 10.14, 10.18 and 10.T, T being terephthalic acid, said minor monomer representing from 1% to 7% by mass of the total blend of said monomer and wherein the change in the crystallization temperature is at least 5° C.
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