Synthetic surfaces with robust and tunable underwater superoleophobicity

Patent metadata

Field	Value
Publication number	US-10487217-B2
Application number	US-201615192364-A
Country	US
Kind code	B2
Filing date	Jun 24, 2016
Priority date	Jun 24, 2015
Publication date	Nov 26, 2019
Grant date	Nov 26, 2019

Abstract

The present invention provides multilayer polymer films, materials and coatings which exhibit robust underwater superoleophobicity and have remarkable structural functional tolerance to a broad range of physical, chemical, and environmental challenges encountered by surfaces deployed in aqueous or aquatic environments. These materials can be fabricated on surfaces of arbitrary shape, size, and composition and provide straightforward means to manipulate surface chemistry and fine-tune other useful features of the interfacial behavior (e.g., underwater oil-adhesiveness). These materials address key obstacles to the application of non-wetting surfaces and anti-fouling ‘super-phobic’ materials in practical, real-world scenarios.

First claim

The invention claimed is:

1. A method for preventing or reducing fouling by hydrophobic materials on a substrate comprising the steps of:
depositing an anti-fouling superoleophobic material on said substrate, wherein said superoleophobic material comprises a multilayer polymer film attached to said substrate, said multilayer film comprising one or more bilayers,
wherein each bilayer comprises a first polymer layer covalently linked with a second polymer layer, wherein the first polymer layer comprises a functionalized azlactone polymer, wherein at least a portion of residual functional groups in the one or more bilayers is functionalized with a hydrophilic group, and wherein said multilayer polymer film attached to said substrate has nanoscale porosity and is non-wetting to oils when covered with an aqueous liquid.

2. The method of claim 1 wherein said multilayer polymer film comprises 10 or more bilayers.

3. The method of claim 1 wherein said material is superoleophobic at a pH range from 1 to 11.

4. The method of claim 1 wherein the first polymer layer comprises a functionalized azlactone having the formula:

wherein x is 0 or the integers 1 or 2; and each R 1 is independently selected from the group consisting of: hydrogen, alkyl groups, alkenyl groups, alkynyl groups, carbocyclic groups, heterocyclic groups, aryl groups, heteroaryl groups, alkoxy groups, aldehyde groups, ether groups, and ester groups, any of which may be substituted or unsubstituted.

5. The method of claim 1 wherein the first polymer layer comprises a polymer selected from the group consisting of poly(vinyl-4,4-dimethylazlactone), poly(2-vinyl-4,4-dimethy 1-2-oxazolin-5 -one), poly(2-isopropeny 1-4,4-dimethyl-2-oxazolin-5-one), poly(2-viny 1-4,4-diethy 1-2-oxazolin-5-one), poly(2-vinyl-4-ethyl-4-methyl-2-oxazolin-5-one), poly(2-vinyl-4-dodecyl-4-methyl-2-oxazolin-5-one), poly(2-vinyl-4,4-pentamethy lene-2-oxazolin -5 -one), poly (2-viny 1-4-methy 1-4-pheny 1-2-oxazolin -5 -one), poly(2-isopropenyl-4-benzyl-4-methyl-2-oxazolin-5-one), and poly(2-vinyl-4,4-dimethyl-1 ,3-oxazin-6-one).

6. The method of claim 1 wherein the first polymer layer comprises poly(vinyl-4,4-dimethylazlactone) (PVDMA).

7. The method of claim 6 wherein the PVDMA is synthesized in the presence of cyclic azlactone-functionalized oligomers.

8. The method of claim 1 wherein the second polymer layer comprises a primary amine functionalized polymer, an alcohol functionalized polymer, or a thiol functionalized polymer.

9. The method of claim 1 wherein the second polymer layer comprises an optionally functionalized polymer selected from the group consisting of polyolefins, poly(alkyls), poly(alkenyls), poly(ethers), poly(esters), poly(imides), polyamides, poly(aryls), poly(heterocycles), poly(ethylene imines), poly(urethanes), poly(α,β-unsaturated carboxylic acids), poly(α,β-unsaturated carboxylic acid derivatives), poly(vinyl esters of carboxylic acids), poly(vinyl halides), poly(vinyl alkyl ethers), poly(N-vinyl compounds), poly(vinyl ketones), poly(vinyl aldehydes) and any combination thereof.

10. The method of claim 1 wherein at least a portion of residual functional groups in the one or more bilayers is reacted with an amine, hydroxyl group, thiol group, or hydrazine group having the formula R—NH 2 , R—OH, R—SH or R—NHNH 2 , where R is hydrophilic.

11. The method of claim 1 wherein at least a second portion of residual functional groups in the one or more bilayers is reacted with a hydrophobic amine, an amino sugar, an amino alcohol, an amino polyol, glucamine, dimethylaminopropylamine (DMAPA), or combinations thereof.

12. The method of claim 1 wherein at least a portion of the residual functional groups in the one or more bilayers is reacted to form chemically labile amide/ester-, amide/thioester-, or amide/imine-type bonds.

13. The method of claim 1 wherein the multilayer film comprises one or more PVDMA/PEI bilayers, which are further functionalized with D-glucamine.

14. The method of claim 1 wherein the substrate is curved or irregularly shaped.

15. The method of claim 1 wherein the multilayer polymer film, material, or both are at least partially optically transparent.

16. A superoleophobic material comprising:
a) a substrate; and
b) a multilayer polymer film attached to said substrate, said multilayer film comprising one or more bilayers, wherein each bilayer comprises a first polymer layer covalently linked with a second polymer layer,
wherein the first polymer layer comprises a functionalized azlactone polymer,
wherein at least a portion of residual functional groups in the one or more bilayers is functionalized with a hydrophilic group,
wherein said multilayer polymer film attached to said substrate has nanoscale or microscale porosity and is non-wetting to oils when covered with an aqueous liquid.

17. The material of claim 16 wherein said multilayer polymer film has a thickness of 10 μm or less.

18. The material of claim 16 wherein the multilayer film comprises 10 or more bilayers.

19. The material of claim 16 wherein the first polymer layer comprises a functionalized azlactone having the formula:

wherein x is 0 or the integers 1 or 2; and each R 1 is independently selected from the group consisting of: hydrogen, alkyl groups, alkenyl groups, alkynyl groups, carbocyclic groups, heterocyclic groups, aryl groups, heteroaryl groups, alkoxy groups, aldehyde groups, ether groups, and ester groups, any of which may be substituted or unsubstituted.

20. The material of claim 16 wherein the first polymer layer comprises a polymer selected from the group consisting of poly(vinyl-4,4-dimethylazlactone), poly(2-vinyl-4,4-dimethy 1-2-oxazolin-5 -one), poly(2-isopropeny 1-4,4-dimethyl-2-oxazolin-5-one), poly(2-viny 1-4,4-diethy 1-2-oxazolin-5-one), poly(2-vinyl-4-ethyl-4-methyl-2-oxazolin-5-one), poly(2-vinyl-4-dodecyl-4-methyl-2-oxazolin-5-one), poly(2-vinyl-4,4-pentamethy lene-2-oxazolin -5 -one), poly (2-viny 1-4-methy 1-4-pheny 1-2-oxazolin -5 -one), poly(2-isopropenyl-4-benzyl-4-methyl-2-oxazolin-5-one), and poly(2-vinyl-4,4-dimethyl-1 ,3-oxazin-6-one).

21. The material of claim 16 wherein the first polymer layer comprises poly(vinyl-4,4-dimethylazlactone) (PVDMA).

22. The material of claim 16 wherein the second polymer layer comprises a primary amine functionalized polymer, an alcohol functionalized polymer, or a thiol functionalized polymer.

23. The material of claim 16 wherein the second polymer layer comprises an optionally functionalized polymer selected from the group consisting of polyolefins, poly(alkyls), poly(alkenyls), poly(ethers), poly(esters), poly(imides), polyamides, poly(aryls), poly(heterocycles), poly(ethylene imines), poly(urethanes), poly(α,β-unsaturated carboxylic acids), poly(α,β-unsaturated carboxylic acid derivatives), poly(vinyl esters of carboxylic acids), poly(vinyl halides), poly(vinyl alkyl ethers), poly(N-vinyl compounds), poly(vinyl ketones), poly(vinyl aldehydes) and any combination thereof.

24. The material of claim 16 wherein at least a portion of residual functional groups in the one or more bilayers is reacted with an amine, hydroxyl group, thiol group, or hydrazine group having the formula R—NH 2 , R—OH, R—SH or R—NHNH 2 , wh

Assignees

• Wisconsin Alumni Res Found

Inventors

• Lynn David
• MANNA Uttam
• Carter Matthew

Classifications

• C09D5/1681 Primary

  Antifouling coatings characterised by surface structure, e.g. for roughness effect giving superhydrophobic coatings or Lotus effect · CPC title

• C09D179/02

  Polyamines · CPC title

• C09D139/04

  Homopolymers or copolymers of monomers containing heterocyclic rings having nitrogen as ring member · CPC title