IP Library Granted Patent US 7,105,106
Granted Patent B2
US 7,105,106 · App. 10/618,319 · Granted Sep 12, 2006

Liquid crystalline polymers, processes for their manufacture, and articles thereof

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Quick Facts
Patent No.
US 7,105,106
App. No.
10/618,319
Granted
Sep 12, 2006
Kind
B2
Abstract

Thermotropic liquid crystalline polymers are produced by the reaction of a polyester made from an aromatic dicarboxylic acid and a diol, one or more hydroxycarboxylic acids, a stoichiometric excess of an aromatic diol, and a carboxylic acid anhydride. Also disclosed are novel liquid crystalline polymers that may be produced by this process. These liquid crystalline polymers are useful as molding resins and shaped articles thereof are produced. In particular, the articles include films, sheets, containers and portions thereof comprising these LCPs.

Claims (52)

1. A process for the manufacture of a liquid crystalline polymer comprising:

(a) contacting, in the absence of added solvent, a partially aromatic polyester, having repeat units of the formula

 and

—O—R 2 —O—  (II),

 with one or more compounds of the formula HO—R 3 —CO 2 H (III), one or more compounds of the formula HO—R 4 —OH (IV), and a carboxylic acid anhydride, under conditions to form esters of (III) and (IV) by reaction with said carboxylic add anhydride, and

(b) heating the mixture resulting from (a) at a temperature and for a sufficient amount of time to form a liquid crystalline polymer wherein

each R 1 is independently hydrocarbylene or substituted hydrocarbylene;

each R 2 is independently alkylene or substituted alkylene;

each R 3 is independently arylene or substituted arylene; and

each R 4 is independently arylene or substituted arylene;

and provided that (IV) is present in an amount, based on the amount of (II) present in said partially aromatic polyester, to achieve a total diol stoichiometric excess of 0.5 to 15 mole percent.

2. The process of claim 1 wherein said carboxylic anhydride is acetic anhydride.

3. The process of claim 2 wherein:

from 90 to 100 mole percent of R 1 is p-phenylene, and from 0 to 10 mole percent of R 1 is m-phenylene;

from 90.0 to 100 mole percent of R 2 is —CH 2 CH 2 — and from 0 to 10.0 mole percent of R 2 is —CH 2 CH 2 OCH 2 CH2—;

(V) is —O—R 4 —O—;

each R4 is 4,4′-biphenylene;

(III) is a mixture of

the molar ratio of (I):[(II)+(V)] is about 1.0:1.0;

the molar ratio of (I):[(IIIA)+(IIIB)] is about 1.0:1.0 to about 1.0:4.0; and

the molar ratio of (IIIA):(IIID) is about 5:1 to about 1:2; and

the stoichiometric excess is 1 to 3 percent.

4. The product of the process of any one of claims 1 , 2 , or 3 .

5. The process as recited in claim 1 comprising the additional step of treating the liquid crystalline polymer with a monomeric functional compound to reduce its melt viscosity at a shear rate of 1000 sec −1 by at least 10%.

6. A container comprising the product of claim 4 .

7. The container of claim 6 that is a pouch or a bag.

8. The container of claim 6 , comprising said liquid crystalline polymer, that is a rigid container selected from the group consisting of a tray, cup, can, bucket, tub, box, pipe, bawl, tube, parison, and carton.

9. The container of claim 8 that is a carton prepared from paperboard extrusion-coated with said liquid crystalline polymer.

10. The container of claim 8 that is a thermoformed multilayer layer cup comprising said liquid crystalline polymer as a barrier layer.

11. The container of claim 10 formed fmm a multilayer structure comprising exterior layers comprising polypropylene and an inner layer comprising said liquid crystalline polymer, with co-extrudable adhesive layers bonding said polypropylene layers to said liquid crystalline polymer layer.

12. A film or sheet comprising the product of any one of claims 1 , 2 or 3 .

13. The film of claim 12 that is a monolayer blown film comprising said liquid crystalline polymer.

14. The film or sheet of claim 12 that is a multilayer structure comprising at least one layer comprising said liquid crystalline polymer.

15. The film or sheet of claim 14 wherein said muitilayer structure comprises exterior layers comprising polypropylene and an inner layer comprising said liquid crystalline polymer, with co-extrudable adhesive layers bonding said polypropylene layers to said liquid crystalline polymer layer.

16. A laminate comprising the film or sheet of claim 12 bonded, by lamination, extrusion coating or co-extrusion coating, to a substrate selected from the group consisting of paper, paperboard, aluminum foil, fabric, nonwoven material, and a film substrate comprising another polymer selected from the group consisting of poly(vinylidene fluoride), nylon-6,6, biaxially oriented polypropylene, biaxially oriented poly(ethylene terephthalate), and polyimide.

17. A laminate comprising kraft paper extrusion coated with the liquid crystalline polymer film or sheet of claim 12 .

18. A laminate comprising paperboard extrusion coated with the liquid crystalline polymer film or sheet of claim 12 .

19. The container of claim 9 which also comprises a heat seal wherein said liquid crystalline polymer forms both sides of said heat seal.

20. The film or sheet of claim 14 that shrinks in any direction more than 4% when heated to 90° C.

21. A process for coating paper with a liquid crystalline polymer, comprising, contacting a surface of a paper sheet with a molten sheet of liquid crystalline polymer to form a coated paper sheet, then while said liquid crystalline polymer on said coated paper sheet is still at least partially molten applying pressure by having a surface which contacts said liquid crystalline polymer on coated paper sheet, said surface having a temperature below a solidification temperature of said liquid crystalline polymer and which applies pressure to said liquid crystalline polymer on coated paper sheet to produce a liquid crystalline polymer coated paper sheet wherein said liquid crystalline polymer is solid.

22. The process as recited in claim 21 , wherein said liquid crystalline polymer comprises a liquid crystalline polymer having repeat units of the formulae

wherein;

each R 1 is independently hydrocarbylene or substituted hydrocarbylene;

each R 2 is independently saturated hydrocarbylene or substituted saturated hydrocarbylene;

each R 4 is independently arylene or substituted arylene;

(V) is about 0.4 to about 32 mole percent of the total of (I) present;

the molar ratio of (I):[(II)+(V)] is about 1.0:1.0;

the molar ratio of (I):[(IIIA)+(IIIB)] is about 1.0:1.0 to about 1.0:4.0; and

the molar ratio of (IIIA):(IIIB) is about 5:1 to about 1:2.

23. The process as recited in claim 21 wherein said suface is one or two quench rolls.

24. The product of the process of claim 21 .

25. A container comprising the product of claim 24 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2019
From: E.I. DU PONT DE NEMOURS AND COMPANY
To: PERFORMANCE MATERIALS NA, INC.
Reel/Frame 050127/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2003
From: SAMUELS, MICHAEL ROBERT; URADNISHECK, JULIUS; WAGGONER, MARION G.
To: E.I. DU PONT DE NEMOURS AND COMPANY
Reel/Frame 014106/0804 →