Composite polyelectrolyte films for corrosion control

• US 20040265603A1
• Filed: 07/29/2004
• Published: 12/30/2004
• Est. Priority Date: 08/03/2001
• Status: Abandoned Application

• Current Assignee: FSU Research Foundation, Inc.
• Original Assignee: FSU Research Foundation, Inc.
• Inventors: Schlenoff, Joseph B
• Application Number:
  US10/485,704
• Publication Number:
  US 20040265603A1
• Time in Patent Office: Days
• US Class Current: 428/461
• CPC Class Codes: C09D 5/08 Anti-corrosive paints
• CPC Class Codes: Y10T 428/31678 Of metal
• CPC Class Codes: Y10T 428/31692 Next to addition polymer from unsaturated monomers

Abstract

A corrosion resistant structure and a method for preparing the same. The corrosion resistant structure comprises a metallic substrate comprising a surface and an anticorrosion polymer coating deposited onto at least a portion of the metallic substrate surface. The anticorrosion polymer coating comprises a polyelectrolyte complex which comprises a positively-charged polyelectrolyte and a negatively-charged polyelectrolyte.

Claims

1. A corrosion resistant structure comprising:

a metallic substrate comprising a surface; and

an anticorrosion polymer coating deposited onto at least a portion of the metallic substrate surface, the anticorrosion polymer coating comprising a polyelectrolyte complex, the polyelectrolyte complex comprising a positively-charged polyelectrolyte and a negatively-charged polyelectrolyte.

2. The corrosion resistant structure of claim 1 wherein the positively-charged polyelectrolyte and the negatively-charge polyelectrolyte are selected from the group consisting of linear polyelectrolytes, branched polyelectrolytes, dendritic polyelectrolytes, graft polyelectrolytes and copolymers and block copolymers thereof.

3. The corrosion resistant structure of claim 1 wherein the positively-charged polyelectrolyte comprises a quaternary ammonium group.

4. The corrosion resistant structure of claim 3 wherein the positively-charged polyelectrolyte is selected from the group consisting of poly(diallyldimethylammonium chloride), poly(vinylbenzyltrimethylammonium), ionenes, poly(acryloxyethyltrimethyl ammonium chloride), poly(methacryloxy(2-hydroxy)propyltrimethyl ammonium chloride), protonated amines and copolymers thereof.

5. The corrosion resistant structure of claim 1 wherein the positively-charged polyelectrolyte comprises a pyridinium group.

6. The corrosion resistant structure of claim 5 wherein the positively-charged polyelectrolyte is selected from the group consisting of poly(N-methylvinylpyridine), other poly(N-alkylvinylpyridines), poly(N-octyl-4-vinyl pyridinium iodide), poly(N-octadecyl-2-ethynyl pyridinium bromide)(PNO2EPB), poly(N-alkyl-2-ethynyl pyridine), poly(N-alkl-4-ethynyl pyridine) and copolymers thereof.

7. The corrosion resistant structure of claim 1 wherein the negatively-charged polyelectrolyte comprises a sulfonate group.

8. The corrosion resistant structure of claim 7 wherein the negatively-charged polyelectrolyte is selected from the group consisting of poly(styrene sulfonate), poly(2-acrylamido-2-methyl-1-propane sulfonate), sulfonated poly(ether ether ketone), sulfonated lignin, poly(ethylenesulfonate), poly(methacryloxyethylsulfonate), sulfonated styrene block copolymers, their salts, and copolymers thereof.

9. The corrosion resistant structure of claim 1 wherein the negatively-charged polyelectrolyte is poly(acrylic acid).

10. The corrosion resistant structure of claim 1 wherein the anticorrosion coating comprises metallic oxide particles.

11. The corrosion resistant structure of claim 10 wherein the metallic oxide particles are selected from the group consisting of silicon dioxide, aluminum oxide, titanium dioxide, iron oxide, zirconium oxide and mixtures thereof.

12. A method for preparing a corrosion resistant structure, the method comprising:

a. providing a metallic substrate comprising a surface; and

b. depositing onto at least a portion of the metallic substrate surface an anticorrosion polymer coating, the anticorrosion polymer coating comprising a polyelectrolyte complex, the polyelectrolyte complex comprising a positively-charged polyelectrolyte and a negatively-charged polyelectrolyte.

13. The method as set forth in claim 12 wherein depositing the anticorrosion polymer coating comprises:

i. applying a first solution comprising a first polyelectrolyte onto the portion of the surface of the metallic substrate whereby the polyelectrolyte in the first solution is adsorbed onto the portion of the metallic substrate surface to form a first polymer layer comprising the first polyelectrolyte;

ii. applying a second solution comprising a second polyelectrolyte that is oppositely-charged from the first polyelectrolyte whereby the second polyelectrolyte is adsorbed onto the first polymer layer to form a second polymer layer comprising the second polyelectrolyte; and

iii. performing steps i and ii until the desired number of first and second polymer layers are formed.

14. The method as set forth in claim 13 comprising rinsing each first and second polymer layer with a rinsing liquid prior to applying the next first or second solution, the rinsing liquid being free of polyelectrolyte and comprising a solvent for the polyelectrolyte in the layer being rinsed.

15. The method as set forth in claim 14 wherein the polyelectrolyte rinsed from each layer is reintroduced into the solution from which it came.

16. The method as set forth in claim 14 comprising drying each rinsed layer prior to applying the next layer.

17. The method as set forth in claim 14 wherein the first and second solutions comprise about 0.01% to about 40% by weight of the first and second polyelectrolytes, respectively.

18. The method as set forth in claim 14 wherein the first and second solutions comprise about 0.1% to about 10% by weight of the first and second polyelectrolytes, respectively.

19. The method as set forth in claim 13 wherein the first polyelectrolyte and the second polyelectrolyte is a positively-charged polyelectrolyte comprising an ammonium group, a pyridinium group or a protonated amine, or a negatively-charged polyelectrolyte comprising a sulfonate group, acrylic acid or a deprotonated carboxylate.

20. The method as set forth in claim 19 wherein the negatively-charged polyelectrolyte comprising a sulfonate group is selected from the group consisting of poly(styrenesulfonic acid), poly(2-acrylamido-2-methyl-1-propane sulfonic acid), sulfonated poly (ether ether ketone), sulfonated styrene block copolymers, sulfonated lignin, poly(ethylenesulfonic acid), poly(methacryloxyethylsulfonic acid), their salts, and copolymers thereof;

the negatively-charged polyelectrolyte comprising acrylic acid is selected from the group consisting of polyacrylic acid and polymethacrylic acid;

the positively-charged polyelectrolyte comprising an ammonium group is selected from the group consisting of poly(diallyldimethylammonium chloride), poly(vinylbenzyltrimethylammonium), ionenes, poly(acryloxyethyltrimethyl ammonium chloride), poly(methacryloxy(2-hydroxy)propyltrimethyl ammonium chloride) and copolymers thereof;

the positively-charged polyelectrolyte comprising a pyridinium group is selected from the group consisting of poly(N-methylvinylpyridine), other poly(N-alkylvinylpyridines), poly(N-octyl-4-vinyl pyridinium iodide, poly(N-octadecyl-2-ethynyl pyridinium bromide) and copolymers thereof; and

the positively-charged polyelectrolyte comprising a protonated amine is poly(allylaminehydrochloride).

21. The method as set forth in claim 13 wherein the first and second solutions comprise an additive selected from the group consisting of an inorganic material, a medicinal material, a surface active ion and mixtures thereof, the inorganic material being selected from the group consisting of a metallic oxide, a clay mineral, a metal colloid, semiconductor nanoparticles and mixtures thereof, the medicinal material being selected from the group consisting of an antibiotic, an antiviral, an antifungal, a coagulant, a steroid, a biocompatibilizer, a sterilizer, an anticoagulant and mixtures thereof, and the surface active ion being selected from the group consisting of stearic acid, sodium stearate, sodium dodecyl sulfate, a quaternary alkyl ammonium and mixtures thereof.

22. The method as set forth in claim 13 wherein the first solution comprises metallic oxide particles selected from the group consisting of silicon dioxide, aluminum oxide, iron oxide, titanium dioxide, zirconium oxide and mixtures thereof.

23. The method as set forth in claim 13 wherein the second solution comprises metallic oxide particles selected from the group consisting of silicon dioxide, aluminum oxide, iron oxide, titanium dioxide, zirconium oxide and mixtures thereof.

24. The method as set forth in claim 13 wherein the first and the second solutions are applied by spraying.

25. The method as set forth in claim 13 wherein the first and the second solutions are applied by dip coating.

26. The method as set forth in claim 12 wherein depositing the anticorrosion polymer coating comprises:

i. providing a first solution comprising a positively-charged polyelectrolyte;

ii. providing a second solution comprising a negatively-charged polyelectrolyte;

iii. mixing the first and second solutions to form a polyelectrolyte complex precipitate;

iv. dissolving the polyelectrolyte complex precipitate in a solvent to form a polyelectrolyte complex solution or suspending the polyelectrolyte complex precipitate within a liquid to form a polyelectrolyte complex dispersion; and

v. applying the polyelectrolyte complex solution or the polyelectrolyte complex dispersion onto the portion of the metallic substrate surface whereby the polyelectrolyte complex in the polyelectrolyte complex solution or the polyelectrolyte dispersion is adsorbed onto the portion of the metallic substrate surface to form a polymer layer comprising the polyelectrolyte complex.

27. The method as set forth in claim 26 wherein the first solution comprises metallic oxide particles selected from the group consisting of silicon dioxide, aluminum oxide, iron oxide, titanium dioxide, zirconium oxide and mixtures thereof.

28. The method as set forth in claim 26 wherein the second solution comprises metallic oxide particles selected from the group consisting of silicon dioxide, aluminum oxide, iron oxide, titanium dioxide, zirconium oxide and mixtures thereof.