Novel high molecular weight diimide diacids and modified thermoplastic copolyether ester elastomers prepared therefrom

• US 4,661,582 A
• Filed: 05/05/1986
• Issued: 04/28/1987
• Est. Priority Date: 10/26/1984
• Status: Expired due to Term

• Current Assignee: General Electric Company
• Original Assignee: General Electric Company
• Inventors: McCready, Russell J.
• Primary Examiner(s): Phynes, Lucille M.
• Application Number:
  US06/860,148
• Time in Patent Office: 358 Days
• Field of Search: 528/288, 528/291, 528/292, 528/296, 528/297, 525/408
• US Class Current: 528/292
• CPC Class Codes: C08G 73/16 Polyester-imides

Abstract

Novel diimide diacids and modified polyetherimide esters are prepared therefrom by reacting diols, dicarboxylic acids and a combination of the novel diimide diacid and dimer acid. These compositions have many excellent properties which make them particularly useful for extrusion and molding applications.

Claims

1. The imidization reaction product of

(a) a tricarboxylic acid anhydride or the corresponding acid thereof containing two vicinal carboxyl groups and

(b) a polyoxyalkylene diamine of the formula

View Dependent Claims (2, 3, 4, 5, 6)

2. The reaction product of claim 1 wherein the tricarboxylic acid anhydride is represented by the formula:

##STR3## wherein R a C₂ to C₂₀ organic aliphatic, cycloaliphatic or aromatic trivalent radical having two vicinal reactive sites and R'"'"' is selected from the group consisting of hydrogen, or a monovalent organic radical selected from the group consisting of a C₁ to C₆ aliphatic or cycloaliphatic hydrocarbon radical or a C₆ to C₁₂ aromatic radical.

3. The reaction product of claim 1 wherein the tricarboxylic acid anhydride is trimellitic anhydride.

4. The reaction product of claim 1 wherein the polyoxyalkylene diamine is selected from the group consisting of poly(propylene ether) diamine, poly(tetramethylene ether) diamine and co-poly(ethylene ether-propylene ether) diamine.

5. The reaction product of claim 1 wherein the polyoxyalkylene diamine is poly(propylene ether) diamine.

6. The reaction product of claim 1 wherein the polyoxyalkylene diamine is co-poly-(ethylene ether-propylene ether) diamine have a predominately polyethylene ether backbone.

7. High molecular weight poly ether diamide diacids of the formula:

##STR4## wherein each R is independently selected from the group consisting of C₂ to C₂₀ aliphatic and cycloaliphatic trivalent organic radicals and C₆ to C₂₀ aromatic trivalent organic radicals having two vicinal reactive sites;

each R'"'"' is independently selected from the group consisting of hydrogen, C₁ to C₆ aliphatic and cycloaliphatic monovalent organic radicals and C₆ to C₁₂ aromatic monovalent organic radicals, and G is the radical remaining after removal of the amino groups of a long chain ether diamine having an average molecular weight of from about 600 to 12,000.

8. The diimide diacid of claim 7 wherein R is a trivalent 6 membered aromatic hydrocarbon and R'"'"' is hydrogen.

9. The diimide diacid of claim 7 wherein G is the divalent radical remaining after removal of the terminal amino groups of a long chain ether diamine having a molecular weight of from about 900 to about 4000.

10. The diimide diacid of claim 7 wherein G is the divalent radical remaining after removal of the terminal amino groups of a long chain poly(alkylene ether) diamine selected from the group consisting of poly(ethylene ether) diamine, poly(tetramethylene ether) diamine, and a random or block copoly(ethylene ether-propylene ether) diamine.

11. The diimide diacid of claim 7 wherein G is the divalent radical remaining after removal of the terminal amino groups of poly(propylene ether) diamine.

12. The diimide diacid of claim 7 wherein G is the divalent radical remaining after removal of the terminal amino groups of a co-poly(propylene ether-ethylene ether) diamine.

13. The diimide diacid of claim 12 wherein the co-poly(propylene ether-ethylene ether) diamine has a predominately poly(ethylene ether) backbone.

14. The diimide diacid of claim 8 wherein R is the radical remaining after removal of the carboxylic group of trimellitic acid or trimellitic anhydride, respectively.

15. The diimide diacid of claim 14, wherein R is derived from trimellitic anhydride.