Aqueous fluoromodified polyurethane system for anti-graffiti and anti-soiling coatings

• US 7,501,472 B2
• Filed: 02/26/2003
• Issued: 03/10/2009
• Est. Priority Date: 02/27/2002
• Status: Expired due to Fees

• Current Assignee: Construction Research & Technology GmbH (BASF SE)
• Original Assignee: Construction Research & Technology GmbH (BASF SE)
• Inventors: Stadler, Rupert, Hiller, Wolfgang, Maier, Alois, Wolfertstetter, Franz, Steidl, Norbert
• Primary Examiner(s): SERGENT, RABON A
• Application Number:
  US10/485,617
• Publication Number:
  US 20040192835A1
• Time in Patent Office: 2,204 Days
• Field of Search: 524/591, 524/839, 524/840, 528/49, 528/70, 528/71
• US Class Current: 524/591
• CPC Class Codes: C08F 283/006 on to polymers provided for in C08G18/00 C08F283/004 takes precedence
• CPC Class Codes: C08G 18/0823 containing carboxylate salt groups or groups forming them
• CPC Class Codes: C08G 18/12 using two or more compounds having active hydrogen in the first polymerisation step
• CPC Class Codes: C08G 18/2885 containing halogen atoms
• CPC Class Codes: C08G 18/3271 Hydroxyamines
• CPC Class Codes: C08G 18/3275 containing two hydroxy groups
• CPC Class Codes: C08G 18/3812 having fluorine atoms
• CPC Class Codes: C08G 18/44 Polycarbonates
• CPC Class Codes: C08G 18/6659 with compounds of group C08G18/34
• CPC Class Codes: C09D 175/04 Polyurethanes

Abstract

An aqueous fluoromodified polyurethane system for one- or two-component anti-graffiti and anti-soiling coatings is prepared by (a) preparing a binder component based on an aqueous solution or dispersion of optionally hydroxy- and/or amino-functional oligourethanes and/or polyurethanes having fluorinated side chains, and, optionally, (b) subsequently reacting the binder component with a crosslinker.

Claims

1. An aqueous fluoromodified polyurethane system for one- or two-component anti-graffiti and anti-soiling coatings, prepared by the process comprising the steps of:

(a) preparing a binder component comprising an aqueous solution or dispersion of at least one of an optionally hydroxyl- or amino-functional oligo- or polyurethane having fluorinated side chains, by

(a₁) reacting from 2.5 to 12 parts by weight of a fluoromodifled polyol component (A)(i) having two or more isocyanate-reactive hydroxyl groups and a molecular mass of from 500 to 2,000 daltons, wherein component (A)(i) is at least one of a reaction product or a macromonomer of a monofunctional fluoroalcohol, an aliphatic diisocyanate, an aromatic diisocyanate, or both an aliphatic diisocyanate and an aromatic diisocyanate, and a diethanolamine, wherein the fluoroalcohol is a perfluoroalkyl alcohol having methylene groups of the formula

F(CF₂)_x—

(CH₂)_y—

OH

with x=4-20 and y=1-6

or hexafluoropropene oxide (HFPO) oligomer alcohol of the formula CF₃CF₂CF₂O—

(CF(CF₃)CF₂O)_z—

CF(CF₃)CH₂—

OH,

wherein z is from 1 to 10

or a mixture thereof, from 10 to 50 parts by weight of a high molecular mass polyol component (A)(ii) having two or more polyisocyanate-reactive hydroxyl groups and a molecular mass of from 500 to 6,000 daltons, and from 0 to 10 parts by weight of a low molecular mass polyol component (A)(iii) having two or more polyisocyanate-reactive hydroxyl groups and a molecular mass of from 50 to 499 daltons with from 2 to 30 parts by weight of a polyisocyanate component (B) comprising at least one polyisocyanate having two or more aliphatic or aromatic isocyanate groups or a paint polyisocyanate, and adding from 0 to 25 parts by weight of a solvent component (C) composed of an inert organic solvent, optionally in the presence of a catalyst, to yield a polyurethane preadduct;

(a₂) reacting the polyurethane preadduct from stage (a₁), optionally in the presence of a catalyst, with from 0.1 to 10 parts by weight of a low molecular mass, anionically modifiable polyol component or polyamine component (A) (iv) having two or more polyisocyanate-reactive hydroxyl groups, amino groups or a combination thereof and one or more inert carboxylic or sulfonic acid groups, some or all of which are optionally converted by means of bases into at least one of carboxylate or sulfonate groups, respectively, or are already in the form of at least one of carboxylate or sulfonate groups, having a molecular mass of from 100 to 1,000 daltons or with from 0.1 to 20 parts by weight of a polymeric polyol component (A)(v) having two or more polyisocyanate-reactive hydroxyl groups and further, polyisocyanate-inert, hydrophilic groups, having a molecular mass of from 500 to 5,000 daltons, to form a polyurethane prepolymer containing free isocyanate groups;

(a₃) optionally reacting the polyurethane prepolymer from stage (a₂) such that some or all of the free isocyante groups are reacted with from 0.1 to 15 parts by weight of a chain terminator component (D) having three or more isocyanato-reactive hydroxyl groups, primary amino groups, secondary amino groups, or a combination thereof that react with the free isocyanate groups of the polyurethane prepolymer from stage (a₂) and wherein component (D) has a molecular mass of from 50 to 500 daltons, to yield a polyfunctional polyurethane oligomer or polymer that is chain terminated or partly chain terminated;

(a₄) admixing the polyfunctional polyurethane oligomer or polymer that is chain terminated or partially chain terminated from stage (a₃) with from 0.1 to 10 parts by weight of a neutralizing component (E) to neutralize some or all of the acid groups to form a neutralized polyurethane oligomer or polymer, and then

(a₅) dispersing the neutralized polyurethane oligomer or polymer that is chain terminated or partially chain terminated from stage (a₄) in from 40 to 120 parts by weight of water to yield a dispersion of neutralized polyurethane oligomer or polymer, wherein said dispersion of the neutralized polyurethane oligomer or polymer optionally contains from 0 to 50 parts by weight of a formulating component (F), and

(a₆) optionally reacting the neutralized polyurethane oligomer or polymer that is partially chain terminated from stage (a₅) with from 0 to 10 parts by weight of a chain extender component (G) having three or more isocyanato-reactive primary amino groups, secondary amino groups, or a combination thereof and a molecular mass of from 50 to 500 daltons, to yield a polyurethane oligomer or polymer having at least one extended chain;

and, optionally,

(b) subsequently reacting the binder component prepared in stage (a₅) or stage (a₆) with from 20 to 100 parts by weight of a crosslinker component (H), wherein said crosslinker component (H) comprises a water-dispersible polyisocyanate having at least two of an aliphatically, cycloaliphatically or aromatically attached isocyanate groups and optionally containing from 0 to20 parts by weight of an organic solvent.

2. The polyurethane system of claim 1, wherein the high molecular mass polyol component (A) (ii) comprises a polyether, polyester, polycaprolactone, polycarbonate-polyol or an α

, ω

-polymethacrylatediol, or a combination thereof.

3. The polyurethane system of claim 2, wherein component A(ii) is a linear, difunctional polyester, polycaprolactone or a polycarbonate-polyol having a molecular mass of from 1,000 to 3,000 daltons.

4. The polyurethane system of claim 1, wherein component (A)(iii) is at least one alcohol selected from the group consisting of 1,4-butanediol, 2-methyl-1,3-propanediol and neopentyl glycol.

5. The polyurethane system of claim 1, wherein component (A) (iv) is a bishydroxyalkanecarboxylic acid, bishydroxy-sulfonic acid, or an alkali metal salt thereof having a molecular mass of from 100 to 1,000 daltons.

6. The polyurethane system of claim 5, wherein the bishydroxyalkanecarhoxylic acid is 2-hydroxymethyl-2-methyl-3-hydroxypropionic or dimethylolpropionic acid.

7. The polyurethane system of claim 1, wherein component (A)(v) is a reaction product of poly(ethylenc oxide [co/block/ran-propylene oxide]) monoalkyl ethers, a diisocyanate, and diethanolamine.

8. The polyurethane system of claim 1, wherein the polyfunctional chain terminator component (D) is an aliphatic polyol, a cycloaliphatic polyol, a polyamine or amino alcohol.

9. The polyurethane system of claim 8, wherein said polyfunctional chain terminator component (D) is selected from the group consisting of diethanolamine, trimethylolpropane, pentaerythritol and a carbohydrate.

10. The polyurethane system of claim 1, wherein the NCO/OH equivalent ratio of components (A) and (B) has a value of from 1.2:

1 to 2.5;

1.

11. The polyurethane system of claim 1, wherein said crosslinker component (H) water-dispersible polyisocyanate having aliphatically, cycloaliphatically or aromatically attached isocyanate groups are used which contain from 0 to 20 parts by weight of an organic solvent.

12. The polyurethane system of claim 1, wherein reaction stages (a₁) and (a₂) are conducted in the presence of from 0.01 to 1% by weight, based on components (A) and (B), of a catalyst for polyaddition reactions with polyisocyanates.

13. The polyurethane system of claim 1, wherein the neutralizing component (E) is added in an amount such that the degree of neutralization, based on the free carboxylic or sulfonic acid groups of the polyurethane oligomer or polymer formed from components (A), (B), (D), (E), and (G), is from 60 to 100 equivalent %.

14. The polyurethane system of claim 1, wherein the chain terminator component (D) is added in an amount such that the level of chain termination, based on the free isocyanate groups of the polyurethane preadduct formed from components (A) and (B) in stage (a₁), is from 0 to 100 equivalent %.

15. The polyurethane system of claim 1, wherein the chain extender component (G) is added in an amount such that the degree of chain extension, based on the free isocyanate groups of the neutralized polyurethane oligomer or polymer formed from components (A), (B), (D), and (E) in stage (a₄), is from 0 to 95 equivalent %.

16. The polyurethane system of claim 1, wherein the solids content in terms of polyurethane oligomer or polymer composed of components (A), (B), (D), (E), and (G) is adjusted to from 35 to 60% by weight, based on the total amount of an aqueous binder component composed of(A) to (E) and (G).

17. The polyurethane system of claim 1, wherein said polyurethane oligomer or polymer having at least one extended chain comprising said components (A), (B), (C), (D), (E) and (G) form micelles having an average particle size of from 10 to 300 nm.

18. The polyurethane system of claim 1, wherein the polyurethane oligomer or polymer comprising components (A), (B), (D), (E), and (G) has an average molecular mass of from 2,000 to 100,000 daltons.

19. The polyurethane system of claim 1, wherein the ratio of crosslinker component (H) to the binder component formed from components (A) to (E) or (A) to (F) is from 1:

3 to 1;

5 by weight.

20. A process for preparing the aqueous polyurethane system of claim 1 comprising:

(a₁) reacting components (A) (i), (A) (ii), (A) (iii), (B) and (C), optionally in the presence of a catalyst, to form a polyurethane preadduct,

(a₂) reacting the polyurethane preadduct from reaction stage (a₁) with components (A) (iv) and (A) (v),

(a₃) optionally reacting the anionically modifiable polyurethane prepolymer from reaction stage (a₂) with component (D)), in each case only one reactive group of component (D) reacting with an isocyanate group of the polyurethane preadduct,

(a₄) reacting the functionalized and anionically modifiable polyurethane oligomer or polymer from reaction stage (a₃), which optionally has two or more reactive groups per chain end and a total functionality of >

4, with component (E) for complete or partial neutralization, and subsequently

(a₅) dispersing the functionalized and anionically modified polyurethane oligomer or polymer from reaction stage (a₄) in water, which optionally additionally comprises component (F), to yield a chain terminated or partially chain terminated, functionalized, and anionically modified polyurethane oligomer or polymer,

(a₆) optionally reacting the partially chain terminated, functionalized, and anionically modified polyurethane oligomer or polymer from stage (a₅) with component (G), and optionally

(b) reacting the binder component from reaction stage (a₅) or reaction stage (a₆) with the crosslinker component (H), the crosslinker component (H) being added to the binder component and, following application, a crosslinked anti-graffiti and anti-soiling coating system being obtained.

21. The process of claim 20, wherein stages (a₄) and (a₅) are integrated with one another such that component (E) is added to the water prior to dispersing.

22. The process of claim 20, wherein stages (a₅) and (a₆) are integrated with one another such that component (G) is added to the water prior to dispersing.

23. The process of claim 20, wherein reaction stages (a₁) to (a₃) are conducted at a temperature of from 60 to 120°

C.

24. The process of claim 20, wherein reaction stage (a₄) is conducted at a temperature of from 40 to 65°

C.

25. The process of claim 20, wherein reaction stages (a₅) and (a₆) are conducted at from 30 to 50°

C.

26. The process of claim 20, wherein reaction stage (b) is conducted at a temperature of from 20 to 40°

C.

27. A mineral building material comprising the aqueous fluoromodifled one- or two-component polyurethane system of claim 1.

28. The mineral building material of claim 27, wherein the polyurethane system is provided in a system for dirt-repellent anti-graffiti coatings on plastic, wood or metal.

29. The polyurethane system of claim 1, wherein said formulating component (F) comprises at least one member selected from the group consisting of a defoamer, a devolatilizer, a lubricant and leveling additive, a radiation curing additive, a dispersing additive, a substrate wetting additive, a hydrophobicizing agent, a rheological additive, a coalescence aid, a flatting agent, an adhesion promoter, an antifreeze agent, an antioxidant, a UV stabilizer, a bactericide, a fungicide, a further polymer, a further polymer dispersion, a filler, a pigment, and a flatting agent.