Thermoplastic structure for transporting refrigerant fluid
US-2015376335-A1 · Dec 31, 2015 · US
US12384883B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12384883-B2 |
| Application number | US-201917282067-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 2, 2019 |
| Priority date | Oct 3, 2018 |
| Publication date | Aug 12, 2025 |
| Grant date | Aug 12, 2025 |
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A process for manufacturing a transparent polyamide including a step of polycondensation of a mixture of monomers including at least one dicarboxylic acid and at least one cycloaliphatic diamine, in which the cycloaliphatic diamine includes two rings linked by an alkylene group including 1 to 6 carbon atoms, each ring being substituted by an amine group and at least one alkyl group, which may be identical or different, including 1 to 6 carbon atoms, wherein the diamine decomposes into six isomer fractions when it is subjected to analysis by gas chromatography on a nonpolar column and, when the isomer fractions are named isomer fractions I to VI in their order of elution, the mass content F I of fraction I of the cycloaliphatic diamine does not exceed 35%. A transparent polyamide capable of being obtained by the process, and to articles obtained from such a polyamide or from such a formulation.
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The invention claimed is: 1. A process for manufacturing a transparent polyamide comprising a step of polycondensation of a mixture of monomers comprising at least one dicarboxylic acid and at least one cycloaliphatic diamine, in which the cycloaliphatic diamine comprises two rings linked by an alkylene group comprising 1 to 6 carbon atoms, each ring being substituted by an amine group and at least one alkyl group, which may be identical or different, comprising 1 to 6 carbon atoms, wherein the diamine decomposes into six isomer fractions when it is subjected to analysis by gas chromatography on a nonpolar column and wherein, when said isomer fractions are named isomer fractions I to VI in their order of elution, the mass content F I of fraction I of said cycloaliphatic diamine does not exceed 33%, wherein the dicarboxylic acid is a mixture of terephthalic acid and isophthalic acid comprising at least 50 mol % of terephthalic acid, wherein the cycloaliphatic diamine is bis(3-methyl-4-aminocyclohexyl)methane and the polycondensation is carried out in the presence of lauryllactam or aminoundecanoic acid. 2. The process as claimed in claim 1 , in which at least one cycloaliphatic diamine is characterized by a mass content of isomer fraction F II which is greater than its mass content of isomer fraction F I . 3. The process as claimed in claim 1 , in which the at least one cycloaliphatic diamine is characterized by a difference ΔF II/I between the mass content of isomer fraction II and isomer fraction I which is greater than 0%. 4. The process as claimed in claim 1 , in which the dicarboxylic acid is a mixture of terephthalic acid and isophthalic acid comprising at least 60 mol % of terephthalic acid. 5. The process as claimed in claim 1 , in which the polycondensation is carried out in the presence of aminoundecanoic acid. 6. The process as claimed in claim 1 , in which the polycondensation is carried out in the presence of lauryllactam. 7. A transparent polyamide obtained by the process as claimed in claim 1 . 8. A formulation obtained from a transparent polyamide as claimed in claim 7 via mixing with one or more other polymers, additives, fillers and/or modifiers. 9. Articles obtained from a transparent polyamide as claimed in claim 7 . 10. The process as claimed in claim 1 , in which the dicarboxylic acid is a mixture of terephthalic acid and isophthalic acid comprising at least 75 mol % of terephthalic acid. 11. The process as claimed in claim 1 , in which the mass content F I of fraction I of said cycloaliphatic diamine does not exceed 30%.
derived from amino acids, polyamines and polycarboxylic acids · CPC title
from at least two different diamines or at least two different dicarboxylic acids · CPC title
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