Modification of polymer surfaces

• US 5,051,312 A
• Filed: 03/29/1990
• Issued: 09/24/1991
• Est. Priority Date: 03/29/1990
• Status: Expired due to Term

• Current Assignee: E. I. du Pont de Nemours and Company (Corteva, Inc.)
• Original Assignee: E. I. du Pont de Nemours and Company (Corteva, Inc.)
• Inventors: Allmer, Klas G. M.
• Primary Examiner(s): LUSIGNAN, MICHAEL R
• Application Number:
  US07/500,830
• Time in Patent Office: 544 Days
• Field of Search: 427/53.1, 427/54.1, 427/437, 427/2, 522/14, 522/120, 522/126, 522/127, 522/129, 522/134, 264/22, 264/25, 428/458, 428/457, 428/463
• US Class Current: 428/458
• CPC Class Codes: B29C 2035/0827 using UV radiation
• CPC Class Codes: B29C 2035/0833 using actinic light
• CPC Class Codes: B29C 59/16 by wave energy or particle radiation , e.g. infrared heating B29C59/007 takes precedence
• CPC Class Codes: C08J 7/12 Chemical modification
• CPC Class Codes: G01N 33/54353 with ligand attached to the carrier via a chemical coupling agent coatings G01N33/54393
• CPC Class Codes: H05K 1/034 containing halogen
• CPC Class Codes: H05K 2203/1168 Graft-polymerization
• CPC Class Codes: H05K 3/185 by making a catalytic pattern by photo-imaging
• CPC Class Codes: H05K 3/381 by special treatment of the substrate
• CPC Class Codes: Y10T 428/31681 Next to polyester, polyamide or polyimide [e.g., alkyd, glue, or nylon, etc.]
• CPC Class Codes: Y10T 428/31699 Ester, halide or nitrile of addition polymer

Abstract

This invention concerns a process for modifying polymer surfaces by contacting the surface with a selected organic modifying agent while irradiating the surface with ultraviolet and/or visible light that can be absorbed by the modifier. Patterns of modified and unmodified surfaces can be produced. Polymers with modified surfaces are useful for absorbing biologically active molecules, composites, printing plates and electronics.

Claims

1. A process for modifying polymer surfaces, comprising, exposing an organic modifier to actinic radiation while a polymer surface is in contact with said organic modifier, provided that the oxidation potential of the modifier minus the reduction potential of the polymer minus the excitation energy of the modifier is less than zero, further provided that said actinic radiation is of a wavelength that is absorbed by said modifier, further provided said polymer does not contain ethylenic unsaturation, and further provided that such modifier does not modify the polymer surface in the absence of actinic radiation:

2. The process as recited in claim 1 wherein said modifier is in a solution in contact with said polymer surface.

3. The process of claim 2 wherein the concentration of said modifier in said solution is about 0.001 to about 0.2M.

4. The process as recited in claim 3 wherein said concentration is about 0.025 to about 0.1M.

5. The process as recited in claim 2 wherein the solvent is a polar aprotic compound.

6. The process as recited in claim 5 wherein said solvent is selected from the group consisting of N,N-dimethylformamide, dimethylsulfoxide, acetonitrile, and dimethylacetamide.

7. The process as recited in claim 1 wherein said modifier is present in the vapor state.

8. The process as recited in claim 1 where said modifier is coated onto said polymer surface.

9. The process as recited in claim 1 wherein said polymer surface is selected from the group consisting of fluorinated polymers, polyimides and polyesters.

10. The process as recited in claim 2 wherein said polymer surface is selected from the group consisting of fluorinated polymers, polyimides and polyesters.

11. The process as recited in claim 9 wherein said polymer surface is a perfluorinated polymer.

12. The process as recited in claim 10 wherein said polymer surface is a perfluorinated polymer.

13. The process as recited in claim 11 wherein said polymer surface is a perfluorinated polymer or copolymer of tetrafluoroethylene.

14. The process as recited in claim 12 wherein said polymer surface is a perfluorinated polymer or copolymer of tetrafluoroethylene.

15. The process as recited in claim 1 wherein said polymer surface and said modifier are selected from the group consisting of:

perfluorinated polymers and copolymers of tetrafluoroethylene with the 4-hydroxybenzenethiol dianion, p-aminobenzenethiol anion, benzenethiol anion, the dianion of HSCHRCHROH where R is hydrogen or methyl, the anion of 2,5-pentanedione, the anion of diphenylcarbinol, 2-mercaptoethanol, tetrachlorohydroquinone, 4-aminofluorene, phenylthiazine, cis-stilbene, vanillin, the anion of 2-mercaptoethanol, the anion of 2-naphthol, the anion of dibenzoylmethane, the dianion of ethylene glycol, and N,N,N'"'"'N'"'"'-tetramethyl-p-phenylenediamine;

polyimide based on oxydianiline and pyromellitic anhydride with 4-aminofluorene, the dianion of ethylene glycol, the dianion of 3-hydroxybutane-3-thiol, and vanillin;

poly(ethylene terephthalate) with the anion of 4-aminobenzenethiol; and

a copolymer of TFE with perfluoro(2,2-dimethyl-1,3-dioxole) with N,N,N'"'"',N'"'"'-tetramethyl-p-phenylenediamine.

16. The process as recited in claim 2 wherein said polymer surface and said modifier are selected from the group consisting of:

perfluorinated polymers and copolymers of tetrafluoroethylene with the 4-hydroxybenzenethiol dianion, p-aminobenzenethiol anion, benzenethiol anion, the dianion of HSCHRCHROH where R is hydrogen or methyl, the anion of 2,5-pentanedione, the anion of diphenylcarbinol, 2-mercaptoethanol, tetrachlorohydroquinone, 4-aminofluorene, phenylthiazine, cis-stilbene, vanillin, the anion of 2-mercaptoethanol, the anion of 2-naphthol, the anion of dibenzoylmethane, the dianion of ethylene glycol, and N,N,N'"'"'N'"'"'-tetramethyl-p-phenylenediamine;

polyimide based on oxydianiline and pyromellitic anhydride with 4-aminofluorene, the dianion of ethylene glycol, the dianion of 3-hydroxybutane-3-thiol, and vanillin;

poly(ethylene terephthalate) with the anion of 4-aminobenzenethiol; and

a copolymer of TFE with perfluoro(2,2-dimethyl-1,3-dioxole) with N,N,N'"'"',N'"'"'-tetramethyl-p-phenylenediamine.

17. The process as recited in claim 1 wherein an accelerator is present, and provided that said actinic radiation is of a wavelength that is absorbed by said accelerator and/or said modifier.

18. The process as recited in claim 2 wherein an accelerator is present, and provided that said actinic radiation is of a wavelength that is absorbed by said accelerator and/or said modifier.

19. The process as recited in claim 17 wherein said accelerator is selected from the group consisting of benzophenone, thioxanthon and naphthalene.

20. The process as recited in claim 18 wherein said accelerator is selected from the group consisting of benzophenone, thioxanthon and naphthalene.

21. The process as recited in claim 1 wherein said modifier oxidation potential minus said reduction potential of the polymer minus said excitation energy of the modifier is more negative than -0.5 volt.

22. The process as recited in claim 2 wherein said modifier oxidation potential minus said reduction potential of the polymer minus said excitation energy of the modifier is more negative than -0.5 volt.

23. The process as recited in claim 1 wherein a pattern of modified and unmodified polymer surface is created.

24. The process as recited in claim 2 wherein a pattern of modified and unmodified polymer surface is created.

25. The process as recited in claim 7 wherein a pattern of modified and unmodified polymer surface is created.

26. The process as recited in claim 1 wherein said polymer surface is modified to varying degrees.

27. The process as recited in claim 2 wherein said polymer surface is modified to varying degrees.

28. The process as recited in claim 7 wherein said polymer surface is modified to varying degrees.

29. The product of the process of claim 1.

30. The product of the process of claim 2.

31. The product of the process of claim 7.

32. The product of the process of claim 1 used to immobilize biologically active molecules.

33. The process as recited in claim 2 wherein said solvent is water or an alcohol.

34. The process as recited in claim 1 comprising the further step of metalizing the modified polymer surface.

35. The product of the process of claim 34.

36. The process of claim 15 wherein said polymer is a copolymer of TFE with perfluoro(2,2-dimethyl-1,3-dioxole) and said modifier is N,N,N'"'"',N'"'"'-tetramethyl-p-phenylenediamine.

37. The process of claim 16 wherein said polymer surface is a copolymer of TFE with perfluoro(2,2-dimethyl-1,3-dioxole) and said modifier is N,N,N'"'"', N'"'"'-tetramethyl-p-phenylenediamine.