IP Library Granted Patent US 8,524,854
Granted Patent B2
US 8,524,854 · App. 13/059,691 · Granted Sep 3, 2013

Chloro-substituted polyetherimides having improved relative thermal index

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Quick Facts
Patent No.
US 8,524,854
App. No.
13/059,691
Granted
Sep 3, 2013
Kind
B2
Abstract

A polyetherimide having an OH content that is greater than 0 and equal or less than 100 ppm; a Relative Thermal Index that is greater than or equal to 170° C.; and a chlorine content that is greater than 0 ppm is disclosed herein. A method for preparing the polyetherimide is also disclosed.

Claims (48)

1. A polyetherimide comprising a structural unit of Formula (I):

wherein R and R′ can be a linear or cyclic C 2 to C 20 alkyl group or a substituted or unsubstituted C 6 to C 30 aryl group, n has a value of 1 to 40,

wherein the polyetherimide has an OH content that is greater than 0 and less than or equal to 100 parts per million by weight (ppm);

wherein the polyetherimide has a Relative Thermal Index that is greater than or equal to 170° C. measured using the protocol UL746B; and

wherein the polyetherimide has a chlorine content that is greater than 0 ppm.

2. The polymer of claim 1 , wherein chlorine content is present in an amount greater than 0 to 4,000 ppm.

3. The polymer of claim 1 , wherein the polyetherimide has a flame retardant rating of V0 at 1.5 mm.

4. The polymer of claim 3 , wherein the polyetherimide has a flame retardant rating of V0 at 0.8 mm.

5. A composition comprising the polyetherimide of claim 1 and an additional polymer.

6. The composition of claim 5 , wherein the additional polymer is selected from the group consisting of polyesters, polycarbonates, polyolefins, polysulfones, polyphenylene sulfides, polyetheretherketones, polyethersulfones, polyamides, polyamideimides, and combinations thereof.

7. The polyetherimide of claim 1 having the structural unit of Formula (III):

wherein n is an integer having a value of 1 to 40.

8. A composition comprising the polyetherimide of claim 7 and an additional polymer.

9. The composition of claim 8 , wherein the additional polymer is selected from the group consisting of polyesters, polycarbonates, polyolefins, polysulfones, polyphenylene sulfides, polyetheretherketones, polyethersulfones, polyamides, polyamideimides, and combinations thereof.

10. A method for preparing the polyetherimide of claim 1 , which comprises

contacting, in o-dichlorobenzene or anisole as diluent, substantially equimolar amounts of

a disodium salt of a dihydroxy compound of formula HO—R′—OH, and

a slurry of a bisimide, in the presence of a catalytically active amount of a phase transfer catalyst, thereby polymerizing the bisimide and the disodium salt;

wherein the bisimide and the disodium salt are polymerized in the presence of a base selected from alkali metal carbonates, alkyl hydrides, alkali metal hydroxides, alkali metal phosphates, alkali metal bicarbonates, alkali metal acetates, and combinations thereof;

wherein said slurry of bisimide comprises the reaction product of a mixture comprising a diamine of formula H 2 N—R—NH 2 ; chlorophthalic anhydride; and o-dichlorobenzene or anisole; and an optional imidization catalyst, said mixture having a solids content of greater than or equal to about 5% by weight;

wherein the base is added in an amount that is sufficient to produce the polyetherimide of claim 1 .

11. The method of claim 10 , wherein the bisimide is made by reacting chlorophthalic anhydride and excess amount of diamine or a stoichiometric amount of diamine.

12. The method of claim 10 , wherein the method further comprises adding a capping agent and capping amine groups.

13. The method of claim 12 , wherein the capping agent is selected from the group consisting of chlorophthalic anhydrides, phthalic anhydrides, substituted phthalic anhydrides, alkyl anhydrides, cyclic alkyl anhydrides, substituted aryl anhydrides, acyl alkyl halides, acyl aryl halides, aldehydes, ketones, esters, isocyanates, chloroformates, sulfonyl chlorides, and combinations thereof.

14. The method of claim 10 , wherein the disodium salt has excess sodium hydroxide and is caustic rich.

15. The method of claim 10 , wherein the base is K 3 PO 4 .

16. The method of claim 15 , wherein the K 3 PO 4 is added in the form of solid or an aqueous solution.

17. The method of claim 16 , wherein the K 3 PO 4 is added in an aqueous solution and the K 3 PO 4 is dried with bisphenol A disodium salt or 1,3-bis[N-(4-chlorophthalimido)]benzene prior to addition to the slurry.

18. The method of claim 16 , wherein the K 3 PO 4 is added as a solid.

19. The method of claim 18 , wherein the K 3 PO 4 added has a particle size of greater than 0 to 400 microns.

20. The method of claim 19 , wherein the K 3 PO 4 added has a particle size ranging greater than 0 to less than 75 microns.

21. The method of claim 13 , wherein the alkali metal hydroxide is sodium hydroxide.

22. The method of claim 10 , wherein the disodium salt is a bisphenol A disodium salt, the bisimide slurry is a slurry of 1,3-bis[N-(4-chlorophthalimido)]benzene, and the phase transfer catalyst is hexaalkylguanidinium chloride wherein said slurry of 1,3-bis[N-(4-chlorophthalimido)]benzene comprises the reaction product of a mixture comprising m-phenylenediamine; 4-chlorophthalic anhydride; and o-dichlorobenzene or anisole; and an optional imidization catalyst, said mixture having a solids content of greater than or equal to about 5% by weight.

23. A polymer comprising a polyetherimide having the structure of Formula (III):

wherein the polyetherimide has an OH content that is greater than 0 and equal or less than 100 ppm;

wherein the polyetherimide has a Relative Thermal Index that is greater than or equal to 170° C. measured using the protocol UL746B; and

wherein the polyetherimide has a chlorine content that is greater than 0 and less than or equal to 4000 ppm;

wherein the polyetherimide is made by a method comprising

contacting, in o-dichlorobenzene or anisole as diluent, substantially equimolar amounts of bisphenol A disodium salt and a slurry of 1,3-bis[N-(4-chlorophthalimido)]benzene, in the presence of a catalytically active amount of a hexaalkylguanidinium chloride as a phase transfer catalyst, thereby polymerizing the 1,3-bis[N-(4-chlorophthalimido)]benzene and the bisphenol A disodium salt;

wherein the 1,3-bis[N-(4-chlorophthalimido)]benzene and the bisphenol A disodium salt are polymerized in the presence of a base selected from the group consisting of alkali metal carbonates, alkyl hydrides, alkali metal phosphates, alkali metal bicarbonates, alkali metal hydroxides, alkali metal acetates, and combinations thereof;

wherein said slurry of 1,3-bis[N-(4-chlorophthalimido)]benzene comprises the reaction product of a mixture comprising m-phenylenediamine; 4-chlorophthalic anhydride; and o-dichlorobenzene or anisole; and an optional imidization catalyst, said mixture having a solids content of greater than or equal to about 5% by weight

wherein the base is added in an amount that is sufficient to produce the polyetherimide of claim 1 .

24. An article comprising the polymer of claim 1 .

25. An article comprising the polymer of claim 7 .

26. An article comprising the composition of claim 5 .

27. An article comprising the composition of claim 8 .

28. A composition comprising the polyetherimide of claim 1 and a polyimide other than the polyetherimide of claim 1 .

29. A composition comprising the polyetherimide of claim 7 and a polyimide other than the polyetherimide of claim 7 .

Assignments (6)
CORRECTIVE ASSIGNMENT TO CORRECT THE REMOVE THE APPLICATION NUMBER 15039474 PREVIOUSLY RECORDED AT REEL: 054528 FRAME: 0467. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 23, 2021
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 057453/0680 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 26, 2020
From: SABIC GLOBAL TECHNOLOGIES B.V.
To: SHPP GLOBAL TECHNOLOGIES B.V.
Reel/Frame 054528/0467 →
CHANGE OF NAME Recorded Jun 6, 2016
From: SABIC INNOVATIVE PLASTICS IP B.V.
To: SABIC GLOBAL TECHNOLOGIES B.V.
Reel/Frame 038883/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 12, 2011
From: ODLE, ROY RAY
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 026269/0132 →
CORRECTIVE ASSIGNMENT TO CORRECT THE EXECUTION DATE OF MATTHEW L. KULMAN PREVIOUSLY RECORDED ON REEL 026042 FRAME 0910. ASSIGNOR(S) HEREBY CONFIRMS THE EXECUTION DATE SHOULD BE CHANGED FROM 03/04/2011 TO 03/09/2011. Recorded Apr 22, 2011
From: CHIONG, HENDRICH; GUGGENHEIM, THOMAS LINK; KHOURI, FARID FOUAD; KUHLMAN, MATTHEW L.; NAVARRO DE CASTRO, MIGUEL ANGEL; SMITH, BRENNAN A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 026168/0834 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2011
From: CHIONG, HENDRICH; GUGGENHEIM, THOMAS LINK; KHOURI, FARID FOUAD; KUHLMAN, MATTHEW L.; NAVARRO DE CASTRO, MIGUEL ANGEL; SMITH, BRENNAN A.
To: SABIC INNOVATIVE PLASTICS IP B.V.
Reel/Frame 026042/0910 →