IP Library Granted Patent US 8,927,651
Granted Patent B2
US 8,927,651 · App. 13/639,073 · Granted Jan 6, 2015

High-viscosity polyamide composition

Inventors: Magali Davezac (Lyons, FR); Wojciech Bzducha (Lyons, FR)
Assignee: Rhodia Operations
C08L77/00C08L77/06C08L63/00C08L35/06C08L77/02C08L51/06
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Quick Facts
Patent No.
US 8,927,651
App. No.
13/639,073
Granted
Jan 6, 2015
Kind
B2
Abstract

A high-viscosity polyamide composition including a branched polyamide is described. Also described, is a relationship between a high-viscosity polyamide composition and a composition including a copolyamide of a statistical tree type resulting from a reaction between a multifunctional monomer including at least three reactive functions in order to form an amide function. Further described, are three reactive functions of two different types and bifunctional monomers used in the manufacture of linear polyamides. A resulting copolyamide can have a very low melt flow index relative to the linear polyamide and improved impact resistance properties. Lastly, use of such a composition for extrusion blow-molding articles is described.

Claims (29)

1. A composition obtained by blending at least:

a) one copolyamide having a random tree structure, which results from a reaction between at least:

one polyfunctional monomer corresponding to a general formula I:

(AR 1 )—R—(R 2 B) n   (I)

in which: n is an integer between 2 and 10 (limits included), R 1 and R 2 can be identical or different and represent a covalent bond or an aliphatic, arylaliphatic, aromatic or alkylaromatic hydrocarbon radical, R is a linear or branched aliphatic radical, a substituted or unsubstituted cycloaliphatic radical, a substituted or unsubstituted aromatic radical which can comprise several aromatic rings and/or heteroketones, A represents an amine or amine salt functional group or an acid, ester, acid halide or amide functional group, and B represents another amine or amine salt functional group, when A represents an acid, ester, acid halide or amide functional group, and an acid, ester, acid halide or amide functional group, when A represents an amine or amine salt functional group,

at least one bifunctional monomer of following formula II to IV:

A 1 -R 3 -A 1   (II)

B 1 -R 4 -B 1   (III)

and

A 1 -R 5 -B 1 or the corresponding lactams  (IV)

with optionally at least one monofunctional monomer of formula V or formula VI:

R 6 -B 1   (V),

and

R 7 -A 1   (VI)

in which: A 1 and B 1 respectively represent an acid, ester or acid chloride functional group and an amine or amine salt functional group and R 3 , R 4 , R 5 , R 6 and R 7 represent linear or branched alkyl hydrocarbon radicals, substituted or unsubstituted aromatic hydrocarbon radicals or alkylaryl, arylalkyl or cycloaliphatic hydrocarbon radicals which can comprise unsaturations; and

b) one chain extender.

2. The composition as described by claim 1 , wherein R is an aromatic radical.

3. The composition as described by claim 1 , wherein the monomer of formula (I) is a compound in which A represents the amine functional group, B represents the acid functional group, n is equal to 2, R represents an aromatic radical and R 1 and R 2 represent a covalent bond.

4. The composition as described by claim 1 , wherein the monomer of formula (I) is 5-aminoisophthalic acid.

5. The composition as described by claim 1 , wherein the monomer of formula (I) is 6-aminoundecanedioic acid.

6. The composition as described by claim 1 , wherein the copolyamide exhibits a melt flow index of less than 5 g/10 min, measured at 275° C. under a load of 2160 g.

7. The composition as described by claim 1 , wherein the copolyamide exhibits a distribution index D of the molecular weights of greater than 2.

8. The composition as described by claim 1 , wherein the chain extender is selected from the group consisting of: a dialcohol, a bis-epoxide, a polymer carrying epoxide functional group, a polymer carrying anhydride functional group, a bis-N-acyl bis-caprolactam, a diphenyl carbonate, a bisoxazoline, an oxazolinone, a diisocyanate, an organic phosphite.

9. The composition as described by claim 1 , wherein the composition comprises from 0.01% to 5% by weight of chain extenders for the polyamide, with respect to the total weight of the composition.

10. The composition as described by claim 1 , wherein the composition comprises an impact modifier.

11. The composition as described by claim 8 , wherein the dialcohol is selected from the group consisting of ethylene glycol, propanediol, butanediol, hexanediol and hydroquinone bis(hydroxyethyl) ether.

12. The composition as described by claim 8 , wherein the bis-epoxide is bisphenol A diglycidyl ether.

13. The composition as described by claim 8 , wherein the bis-N-acyl bis-caprolactams is selected from the group consisting of isophthaloyl bis-caprolactam, adipoyl bis-caprolactam and terephthaloy bis-caprolactam.

14. The composition as described by claim 8 , wherein the organic phosphite is a triphenyl phosphite or a caprolactam phosphite.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 5, 2020
From: RHODIA OPÉRATIONS
To: PERFORMANCE POLYAMIDES, SAS
Reel/Frame 051726/0747 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2012
From: DAVEZAC, MAGALI; BZDUCHA, WOJCIECH
To: RHODIA OPERATIONS
Reel/Frame 029482/0860 →
Priority Claims (1)
FR 10 52558 · Apr 6, 2010 · national
Continuity (1)
Related Publication 20130131269A1 · May 23, 2013