Methods and compositions for producing polyimide coatings

• US 4,842,948 A
• Filed: 06/20/1985
• Issued: 06/27/1989
• Est. Priority Date: 06/21/1982
• Status: Expired due to Fees

• Current Assignee: John Gagliani, John V. Long
• Original Assignee: John Gagliani, John V. Long
• Inventors: Gagliani, John, Long, John V.
• Primary Examiner(s): KENDELL, LORRAINE
• Application Number:
  US06/746,858
• Time in Patent Office: 1,468 Days
• Field of Search: 428/473.5, 428/335, 427/207.1
• US Class Current: 428/473.5
• CPC Class Codes: C08J 2379/08 Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
• CPC Class Codes: C08J 9/02 using blowing gases generated by the reacting monomers or modifying agents during the preparation or modification of macromolecules
• CPC Class Codes: Y10T 428/264 Up to 3 mils
• CPC Class Codes: Y10T 428/31721 Of polyimide

Abstract

Methods and compositions for producing imide precursors and polyimide coating and adhesives. Basically a mixture of an oxoimine such as caprolactam, a dianhydride such as 3,3'"'"', 4,4'"'"'-benzophenone tetracarboxylic acid dianhydride and a solvent such as dimethyl formamide is heated to a temperature of about 60° to 120° C. for a suitable period, then the mixture is cooled and a suitable diamine is added to produce the imide precursor. This mixture may be dried to a powder form or may be used directly as a coating or adhesive. The final polyimide is produced by heating the precursor to a suitable temperature over an appropriate period.

Claims

1. A method of forming a coating on a surface which comprises the steps of:

providing a quantity of a solvent;

adding thereto in either order, an aromatic tetracarboxylic acid dianhydride and from just above 0 to 10 moles of an oxoimine per mole of said dianhydride, said oxoimine having the general structure. ##STR4## where x is 4 to 7;

maintaining the resulting mixture at a temperature of from about 30°

to 120°

C.;

stirring said mixture until solution is complete;

cooling the resulting solution to a temperature of from about 20°

to 60°

C.;

adding thereto about 1.0 moles of a diamine per mole of dianhydride;

stirring until solution is complete;

forming a layer of said material having a thickness of up to about 3 mils on a surface; and

heating said material to a temperature of from about 175°

to 320°

C. for from about 30 minutes to 5 hours to form a smooth, adherent coating of a high molecular weight polymer.

2. The method according to claim 1 further including the additional steps of repeating the steps of forming a layer and heating said material at least 3 additional times to produce a thicker substantially flawless and pinhole-free coating.

3. The method according to claim 1 including the additional steps after the addition of said diamine and stirring of:

drying the solution to a powder;

storing said power for a selected period;

dissolving said powder in a solvent to produce a liquid material.

4. The method according to claim 1 including the additional steps after the additional of said diamine and stirring of:

drying the solution to a powder to produce a spreadable dry material.

5. The method according to claim 4 wherein said drying is accomplished by spray drying.

6. The method according to claim 1 wherein said aromatic tetracarboxylic acid dianhydride is selected from the group consisting of 3,3'"'"'4,4'"'"'- benzophenone tetracarboxylic acid dianhydride, pyromellitic dianhydride, and mixtures thereof.

7. The method according to claim 3 wherein said aromatic tetracarboxyic acid dianhydride is selected from the group consisting of 3,3'"'"', 4,4'"'"'- benzophenone tetracarboxylic acid dianhydride, pyromellitic dianhydride, and mixtures thereof.

8. The method according to claim 4 wherein said aromatic tetracarboxylic acid dianhydride is selected from the group consisting of 3,3'"'"', 4,4'"'"'- benxophenone tetracarboxylic acid dianhydride, pyromellitic dianhydride, and mixtures thereof.

9. The method according to claim 1 wherein the ratio of oxomine to dianhydride is from just above 0 to 10 and said oxoimine is selected from the group consisting of caprolactam, 2-pyrrolidone or 2-piperidone and mixture thereof.

10. The method according to claim 3, wherein the ratio of oxomine to dianhydride is from just above 0 to 10 and said oxoimine is selected from the group consisting of caprolactam, 2-pyrrolidone or 2-piperidone and mixture thereof.

11. The method according to claim 4 wherein the ratio of oxomine to dianhydride is from just above 0 to 10 and said oxoimine is selected from the group consisting of caprolactam, 2-pyrrolidone or 2-piperidone and mixture thereof.

12. The method according to claim 1 wherein said oxomine is caprolactam and said dianhydride is 3,3'"'"', 4,4'"'"'-benzophenone tetracarboxylic acid dianhydride.

13. The method according to claim 3 wherein said oxoimine is caprolactam and said dianhydride is 3,3'"'"', 4,4'"'"'-benzophenone tetracarboxylic acid dianhydride.

14. The method according to claim 4 wherein said oxoimine is caprolactam and said dianhydride is 3,3'"'"', 4,4'"'"'-benzophenone tetracarboxylic acid dianhydride.

15. The method according to claim 1 wherein said solvent is dimethyl formamide and said diamine is 4,4'"'"'-diaminodiphenyl methane.

16. The method according to claim 3 wherein said solvent is dimethyl formamide and said diamine is 4,4'"'"'-diaminodiphenyl methane.

17. The method according to claim 4 wherein said solvent is dimethyl formamide and said diamine is 4,4'"'"'-diaminodiphenyl methane.

18. The method according to claim 1 wherein said mixture of oxoimine and dianhydride is initially maintained at a temperature of from about 90°

to 100°

C. until solution is complete, followed by cooling to a temperature of from about 40°

to 50°

C.

19. The method according to claim 3 wherein said mixture of oxoimine and dianhydride is initially maintained at a temperature of from about 90°

to 100°

C. until solution is complete, followed by cooling to a temperature of from about 40°

to 50°

C.

20. The method according to claim 4 wherein said mixture of oxoimine and dianhydride is initially maintained at a temperature of from about 90°

to 100°

C. until solution is complete, followed by cooling to a temperature of from about 40°

to 50°

C.

21. The product produced according to the method of claim 15.

22. The product according to the method of claim 4.

23. The product produced according to the method of claim 1.