Polypropylene multilayer sheet
US-2024009975-A1 · Jan 11, 2024 · US
US9243109B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9243109-B2 |
| Application number | US-201214130148-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 28, 2012 |
| Priority date | Jun 30, 2011 |
| Publication date | Jan 26, 2016 |
| Grant date | Jan 26, 2016 |
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This invention relates to a biaxially stretched product comprising a copolyamide comprising monomeric units of: aliphatic non-cyclic diamines X and aliphatic non-cyclic dicarboxylic acids Y or aliphatic non-cyclic α,ω-amino acids Z, and diamines M and diacids N in an amount between 0.1 to 2 wt % based on the total amount of copolyamide, and in which M and N are cyclic, and wherein the product has been stretched at a temperature of between the glass transition temperature (Tg) and the melting temperature (Tm). A method of preparation is claimed, as well as a multilayer film comprising the biaxially stretched product.
Opening claim text (preview).
The invention claimed is: 1. A biaxially stretched product comprising a copolyamide comprising monomeric units of: (i) aliphatic non-cyclic diamines X and aliphatic non-cyclic dicarboxylic acids Y or aliphatic non-cyclic α,ω-amino acids Z, and (ii) diamines M and diacids N in an amount between 0.1 to 1.5 wt % based on the total amount of copolyamide, and in which M and N are cyclic, wherein the product has been stretched at a temperature of between the glass transition temperature (Tg) and the melting temperature (Tm). 2. The biaxially stretched product according to claim 1 , in which N is selected from the group consisting of isophthalic acid (I), terephthalic acid (T), 4-methylisophthalic acid, 4-tert-butylisophthalic acid, 1,4-naphthalenedicarboxylic acid and 2,6-naphthalenedicarboxylic acid. 3. The biaxially stretched product according to claim 1 , in which M is selected from the group consisting of isophoronediamine (IPD), bis-(p-aminocyclohexane)methane (PACM), 2,2-Di-(4-aminocyclohexyl)-propane, 3,3′-dimethyl-4-4′-diaminodicyclohexylmethane, p-xylylenediamine, m-xylylenediamine, and 3,6-bis(aminomethyl)norbornane. 4. The biaxially stretched product according to claim 1 , wherein (a) M is selected from the group consisting of isophoronediamine (IPD), bis-(p-aminocyclohexane)methane (PACM), 2,2-Di-(4-aminocyclohexyl)-propane, 3,3′-dimethyl-4-4′-diaminodicyclohexylmethane, p-xylylenediamine, m-xylylenediamine, and 3,6-bis(aminomethyl)norbornane, and (b) N is selected from the group consisting of isophthalic acid (I), terephthalic acid (T), 4-methylisophthalic acid, 4-tert-butylisophthalic acid, 1,4-naphthalenedicarboxylic acid and 2,6-naphthalenedicarboxylic acid, cis-1,4-cyclohexanedicarboxylic acid, trans-1,4-cyclohexanedicarboxylic acid, cis-1,3-cyclohexanedicarboxylic acid and trans-1,3-cyclohexanedicarboxylic acid. 5. The biaxially stretched product according to claim 1 , wherein Z is selected from the group consisting of ε-caprolactam, aminodecanoic acid, aminoundecanoic acid and aminododecanoic acid. 6. The biaxially stretched product according to claim 1 , wherein X is selected from the group consisting of 1,4-diaminobutane, diaminopentane and hexamethylene diamine. 7. The biaxially stretched product according to claim 1 , whereinany of the claims 1 to 4 , wherein Y is chosen from the group of 1,6-hexanedioic acid, 1,8-octanedioic acid, 1,9-nonanedioic acid, 1,11-decanedioic acid, undecandioic acid, 1,12-dodecanedioic acid. 8. The biaxially stretched product according to any one of the claims 1 - 4 , wherein Z is ε-caprolactam. 9. The biaxially stretched product according to claim 1 , wherein X is hexamethylene diamine and Y is hexamethylene diacid. 10. The biaxially stretched product according to claim 1 , wherein the monomeric units of cyclic diamines of M is isophorone diamine and the monomeric units of cyclic diacids of N is terephthalic acid. 11. The biaxially stretched product according to claim 1 , wherein Z is ε-caprolactam and wherein M is isophorone diamine and N is terephthalic acid. 12. The biaxially stretched product according to claim 1 , wherein X is 1,4-diaminobutane and Y is an aliphatic non-cyclic dicarboxylic acid with at least 8 carbon atoms. 13. A method for preparation of a biaxially stretched product according to claim 1 , comprising the steps of: (A) preparing a copolyamide comprising: (i) aliphatic non-cyclic diamines X and aliphatic non-cyclic dicarboxylic acids Y or aliphatic non-cyclic α,ω-amino acids Z, and (ii) cyclic diamines M and cyclic diacids N in an amount between 0.1 to 1.5 wt % based on the total amount of copolyamide, and (B) subsequently making a product from the copolyamides followed by stretching the product at a temperature of between the glass transition temperature (Tg) and the melting temperature (Tm) of the copolyamide. 14. A multilayer film comprising at least one layer of the biaxially stretched product according to claim 1 .
biaxial · CPC title
derived from amino acids, polyamines and polycarboxylic acids · CPC title
parallel with the direction of feed · CPC title
Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers · CPC title
derived from polyamines and polycarboxylic acids · CPC title
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