IP Library Patent Application 12181023
Patent Application
App. No. 12/181,023

Crystallizable Polyetherimides, Method of Manufacture, and Articles Derived Therefrom

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Patent No.
US None
App. No.
12/181,023
Abstract

A composition is described, which comprises a crystallizable polyetherimide derived from the polymerization of: (a) a dianhydride component, comprising more than 96.8 mole % of 4,4′-bisphenol A dianhydride or a chemical equivalent thereof; and (b) a diamine component comprising a diamine or a chemical equivalent thereof, wherein the crystallizable polyetherimide has a T m ranging from 250° C. to 400° C. and the difference between the T m and T g of the composition is more than 50° C. Further described are articles, such as fibers, made from the composition, methods for making the composition, methods for making the articles, and methods for using the articles.

Claims (60)

1 . A composition comprising a crystallizable polyetherimide derived from:

(a) a dianhydride component, comprising 96.8 mole % or more of 4,4′-bisphenol A dianhydride or a chemical equivalent thereof; and

(b) a diamine component comprising a diamine or a chemical equivalent thereof;

wherein the crystallizable polyetherimide has a T m from 250° C. to 400° C. and the difference between the T m and T g of the composition is equal to or more than 50° C.

2 . The composition of claim 1 , wherein the diamine component comprises para-phenylenediamine or a chemical equivalent thereof.

3 . The composition of claim 1 , wherein the diamine component consists essentially of para-phenylenediamine or a chemical equivalent thereof.

4 . The composition of claim 1 , wherein the diamine component is p-phenylenediamine and the composition further comprises less than 5.0 mole % of meta-phenylenediamine or a chemical equivalent thereof.

5 . The composition of claim 1 , wherein the diamine component is p-phenylenediamine, and wherein the composition further comprises less than 2.0 mole % of meta-phenylenediamine or a chemical equivalent thereof.

6 . The composition of claim 1 , wherein the diamine component is p-phenylenediamine substantially free of meta-phenylenediamine or a chemical equivalent thereof.

7 . The composition of claim 1 , wherein the diamine is selected from the group consisting of p-phenylenediamine; benzidine; 1,5-diaminonaphthalene; bis(4-aminophenyl)methane; bis(4-aminophenyl)propane; bis(4-aminophenyl)sulfide; bis(4-aminophenyl)sulfone; bis(4-aminophenyl)ether; 4,4′-diaminodiphenylpropane; 4,4′-diaminodiphenylmethane(4,4′-methylenedianiline); 4,4′-diaminodiphenylsulfide; 4,4′-diaminodiphenylsulfone; 4,4′-diaminodiphenylether(4,4′-oxydianiline); 1,5-diaminonaphthalene; 3,3′dimethylbenzidine; 4,3′-diaminodiphenylether; 1,3-bis(4-aminophenoxy)benzene; 4,4′-bis(4-aminophenoxy)biphenyl; chemical equivalents of the foregoing diamines; and combinations thereof.

8 . The composition of claim 1 , wherein the composition further comprises at least one stabilizer.

9 . The composition of claim 8 , wherein the stabilizer is a phosphorous-containing stabilizer.

10 . The composition of claim 1 , having an apparent viscosity, measured at a shear rate of 1000 s −1 , of more than 0 and less than 10,000 poise at a temperature of less than 400° C.

11 . The composition of claim 1 , having a viscosity, measured at a shear rate of 1000 s −1 , of more than 100 and less than 7000 poise at a temperature of less than 400° C.

12 . The composition of claim 1 , wherein a fiber comprising the composition has a tensile strength from 2 to 20 grams per denier.

13 . The composition of claim 1 , wherein a fiber comprising the composition a hot-air shrinkage of less than or equal to 20% after exposure to 260° C. air for 10 minutes.

14 . The composition of claim 1 , wherein a fiber comprising the composition a hot-air shrinkage of less than or equal to 10% after exposure to 260° C. air for 10 minutes.

15 . The composition of claim 1 , wherein the composition further comprises an end-capping agent.

16 . The composition of claim 15 , wherein the endcapping agent is selected from the group consisting of phthalic anhydride, aniline, and combinations thereof.

17 . A fiber comprising

a crystallized polyetherimide composition derived from the polymerization of:

(a) a dianhydride component, comprising more than 96.8 mole % of 4,4′-bisphenol A dianhydride or a chemical equivalent thereof; and

(b) a diamine component comprising a diamine or a chemical equivalent thereof;

wherein the fiber has a T m from 250° C. to 400° C. and the difference between the T m and T g of the fiber is equal to or more than 50° C.

18 . The fiber of claim 17 , wherein the diamine component comprises para-phenylenediamine or a chemical equivalent thereof.

19 . The fiber of claim 17 , wherein the diamine component consists essentially of para-phenylenediamine or a chemical equivalent thereof.

20 . The fiber of claim 17 , wherein the diamine component is p-phenylenediamine, and the composition further comprises less than 5.0 mole % of meta-phenylenediamine or a chemical equivalent thereof.

21 . The fiber of claim 17 , wherein the diamine component is p-phenylenediamine, and the composition further comprises less than 2.0 mole % of meta-phenylenediamine or a chemical equivalent thereof.

22 . The fiber of claim 17 , wherein the diamine is selected from the group consisting of p-phenylenediamine; benzidine; 1,5-diaminonaphthalene; bis(4-aminophenyl)methane; bis(4-aminophenyl)propane; bis(4-aminophenyl)sulfide; bis(4-aminophenyl)sulfone; bis(4-aminophenyl)ether; 4,4′-diaminodiphenylpropane; 4,4′-diaminodiphenylmethane(4,4′-methylenedianiline); 4,4′-diaminodiphenylsulfide; 4,4′-diaminodiphenylsulfone; 4,4′-diaminodiphenylether(4,4′-oxydianiline); 1,5-diaminonaphthalene; 3,3′dimethylbenzidine; 4,3′-diaminodiphenylether; 1,3-bis(4-aminophenoxy)benzene; 4,4′-bis(4-aminophenoxy)biphenyl; chemical equivalents of the foregoing diamines; and combinations thereof.

23 . The fiber of claim 17 , wherein the composition further comprises at least one stabilizer.

24 . The fiber of claim 23 , wherein the stabilizer is a phosphorous-containing stabilizer.

25 . The fiber of claim 17 , wherein the composition further comprises an end-capping agent.

26 . The composition of claim 17 , wherein the endcapping agent is selected from the group consisting of phthalic anhydride, aniline, and combinations thereof.

27 . The fiber of claim 17 , wherein the fiber has a tensile strength from 2 to 20 grams per denier.

28 . The fiber of claim 17 , wherein the fiber has a hot-air shrinkage of less than or equal to 20% after exposure to 260° C. air for 10 minutes.

29 . The fiber of claim 17 , wherein the fiber has a hot-air shrinkage of less than or equal to 10% after exposure to 260° C. air for 10 minutes.

30 . An article comprising a plurality of the fibers of claim 17 .

31 . The article of claim 30 , wherein article is a non-woven fabric.

32 . The article of claim 30 , wherein article is a woven fabric.

33 . A method of making a fiber, comprising

extruding, through an orifice under conditions sufficient to form at least one fiber, a crystallizable polyetherimide composition derived from the polymerization of:

(a) a dianhydride component, comprising more than 96.8 mole % of 4,4′-bisphenol A dianhydride or a chemical equivalent thereof; and

(b) a diamine component comprising a diamine or a chemical equivalent thereof;

wherein the crystallizable polyetherimide has a T m ranging from 250° C. to 400° C. and the difference between the T m and T g of the composition is equal to or more than 50° C.

34 . The method of claim 33 wherein the method further comprises drawing the at least one fiber.

35 . The method of claim 33 , wherein the method further comprises heat-treating the at least one fiber under a constraint effective to crystallize the polyetherimide.

36 . The method of claim 33 , wherein the method further comprises weaving fiber into a fabric.

37 . The method of claim 33 , wherein the method further comprises combining a plurality of the fibers into a yarn and then weaving a fabric from the yarn.

38 . A crystallizable polyetherimide composition derived from the polymerization of:

(a) a dianhydride component, comprising more than 96.8 mole % of 4,4′-bisphenol A dianhydride or a chemical equivalent thereof; and

(b) a diamine component comprising p-phenylene diamine or a chemical equivalent thereof, and having less than 5 mole % meta-phenylenediamine or a chemical equivalent thereof;

wherein the crystallizable polyetherimide composition has

a T m from 250° C. to 400° C.;

a viscosity, measured at a shear rate of 1000 s −1 , of more than 100 and less than 10,000 poise at a temperature of less than 400° C., and further

wherein the difference between the T m and a T g of the crystallizable polyetherimide composition is equal to or greater than 50° C.

39 . The composition of claim 38 , wherein the diamine component consists essentially of para-phenylenediamine or a chemical equivalent thereof.

40 . The composition of claim 38 , wherein the diamine component is p-phenylenediamine and the composition further comprises less than 5.0 mole % of meta-phenylenediamine or a chemical equivalent thereof.

41 . The composition of claim 38 , wherein the composition has a viscosity, measured at a shear rate of 1000 s −1 , of more than 100 and less than 10,000 poise at a temperature of less than 400° C.

42 The composition of claim 38 , wherein the composition further comprises an end-capping agent.

43 . The composition of claim 42 , wherein the endcapping agent is selected from the group consisting of phthalic anhydride, aniline, and combinations thereof.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE 12/116841, 12/123274, 12/345155, 13/177651, 13/234682, 13/259855, 13/355684, 13/904372, 13/956615, 14/146802, 62/011336 PREVIOUSLY RECORDED ON REEL 033591 FRAME 0673. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Aug 29, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033663/0427 →
CORRECTIVE ASSIGNMENT TO CORRECT REMOVE 10 APPL. NUMBERS PREVIOUSLY RECORDED AT REEL: 033591 FRAME: 0673. ASSIGNOR(S) HEREBY CONFIRMS THE CHANGE OF NAME. Recorded Aug 28, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033649/0529 →
CHANGE OF NAME Recorded Aug 22, 2014
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 033591/0673 →
RELEASE OF SECURITY INTEREST Recorded Mar 17, 2014
From: CITIBANK, N.A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 032459/0798 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2008
From: SUSARLA, PRAMEELA; BANSAL, AMITABH; WEI, XIAOLAN; KAILASAM, GANESH; GUGGENHEIM, THOMAS LINK; VENKATARAMAN, KARTHIK; HAGBERG, ERIK C.; ODLE, ROY RAY
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 021530/0225 →