Aqueous, highly cross-linked two-component polyurethane coating system, method for the production and use thereof

• US 7,825,210 B2
• Filed: 04/23/2004
• Issued: 11/02/2010
• Est. Priority Date: 10/25/2001
• Status: Expired due to Fees

• Current Assignee: Construction Research & Technology GmbH (BASF SE)
• Original Assignee: Construction Research & Technology GmbH (BASF SE)
• Inventors: Wolfertstetter, Franz, Maier, Alois, Steidl, Norbert
• Primary Examiner(s): Cano; Milton I
• Assistant Examiner(s): GILLESPIE, BENJAMIN
• Application Number:
  US10/830,743
• Publication Number:
  US 20050027092A1
• Time in Patent Office: 2,384 Days
• Field of Search: 524/591, 524/839, 524/840, 528/60, 528/71, 528/85
• US Class Current: 528/71
• 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 18/3206 aliphatic
• CPC Class Codes: C08G 18/3275 containing two hydroxy groups
• CPC Class Codes: C08G 18/348 Hydroxycarboxylic acids
• CPC Class Codes: C08G 18/4277 Caprolactone and/or substituted caprolactone
• CPC Class Codes: C08G 18/44 Polycarbonates
• CPC Class Codes: C08G 18/6659 with compounds of group C08G18/34
• CPC Class Codes: C08G 18/792 formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
• CPC Class Codes: C09D 175/04 Polyurethanes

Abstract

An aqueous highly cross-linked two-component polyurethane coating system is described with reduced hydrophilicity and improved resistance to chemicals which can be obtained by a) producing a binder component based on an aqueous solution or dispersion of low-molecular hydroxyfunctional and/or aminofunctional oligourethanes or polyurethanes and b) by subsequently reacting the binder component a) with a cross-linking component (H) in a ratio of 3:1 to 5:1, wherein water-dispersible polyisocyanates are used as the cross-linking component (H).

Claims

1. An aqueous cross-linked two-component polyurethane coating system formed by a process comprising:

a) producing a binder component based on an aqueous solution or dispersion of hydroxyfunctional and/or aminofunctional oligourethanes or polyurethanes, wherein

a₁) forming polyurethane preadduct by reacting 10 to 50 parts by weight of a higher-molecular weight polyol component (A)(i) containing two or more hydroxyl groups that are reactive with polyisocyanates and having a molecular mass of 500 to 5000 Daltons and 0 to 5 parts by weight of a low-molecular weight polyol component (A)(ii) containing two or more hydroxyl groups that are reactive with polyisocyanates and having a molecular mass of 50 to 499 Daltons with 2 to 20 parts by weight of a polyisocyanate component (B) comprising at least one polyisocyanate, polyisocyanate derivative or polyisocyanate homologue containing two or more aliphatic or aromatic isocyanate groups with addition of 0 to 6 parts by weight of a solvent component (C), components A and B having an NCO/OH equivalent ratio of 1.25;

1 to 2.5;

1;

a₂) forming polyurethane prepolymer by reacting the polyurethane preadduct formed in step a_l) with 0.1 to 1.5 parts by weight of a low-molecular weight and anionically modifiable polyol component (A)(iii) containing one or more hydroxyl groups that are reactive with polyisocyanates and one or more inert carboxylic acid and/or sulfonic acid group(s) which can be partially or completely converted into carboxylate or sulfonate groups in the presence of bases or are already present in the form of carboxylate and/or sulfonate groups, having a molecular mass of 100 to 499 Daltons and with 0 to 8 parts by weight of a hydroxy functional component (A)(iv) containing two or more hydroxyl groups that are reactive with polyisocyanates and other hydrophilic groups that are inert towards polyisocyanates having a molecular mass of 500 to 5000 Daltons;

a₃) forming a multifunctional polyurethane oligomer or polymer by reacting the free isocyanate groups of the polyurethane prepolymer from step a₂) with 0.1 to 15 parts by weight of a multifunctional chain stopping component (D) containing three or more hydroxyl groups and/or primary and/or secondary amino groups that are reactive with isocyanate groups and having a molecular mass of 50 to 500 Daltons, one of the hydroxyl groups or one of the amino groups reacts with the polyurethane preadduct, the chain stopping component being in an amount that there is no unreacted polyol in a₃ in addition to the oligomer from step a₂ and wherein water dispersion of a₃ is achieved with conversion and hydrophilization to a salt of not more than about 20 meq/(100)g solid resin of ionic groups;

a₄) reacting the multifunctional polyurethane oligomer or polymer from step a₃) with 0.1 to 1 parts by weight of a neutralization component (E) to partially or completely neutralize the acidic groups and to form neutralized polyurethane oligomer or polymer; and

a₅) dispersing the neutralized polyurethane oligomer or polymer from step a₄) in 40 to 60 parts by weight of water which also contains 0 to 50 parts by weight of a formulation component (F) to form a binder component; and

b) reacting the binder component from step a₅) with a cross-linking component (H) in a ratio of 3;

1 to 5;

1, wherein the cross-linking component (H) comprises water-dispersible polyisocyanates containing aliphatically and/or cycloaliphatically and/or aromatically bound isocyanate groups which can contain 0 to 20 parts by weight of an organic solvent.

2. An aqueous cross-linked two-component polyurethane coating system formed by a process comprising:

a) producing a binder component based on an aqueous solution or dispersion of hydroxyfunctional and/or aminofunctional oligourethanes or polyurethanes, wherein

a₁) forming polyurethane preadduct by reacting 10 to 50 parts by weight of a higher-molecular weight polyol component (A)(i) containing two or more hydroxyl groups that are reactive with polyisocyanates and having a molecular mass of 500 to 5000 Daltons and 0 to 5 parts by weight of a low-molecular weight polyol component (A)(ii) containing two or more hydroxyl groups that are reactive with polyisocyanates and having a molecular mass of 50 to 499 Daltons with 2 to 20 parts by weight of a polyisocyanate component (B) comprising at least one polyisocyanate, polyisocyanate derivative or polyisocyanate homologue containing two or more aliphatic or aromatic isocyanate groups with addition of 0 to 6 parts by weight of a solvent component (C), components A and B having an NCO/OH equivalent ratio of 1.25;

1 to 2.5;

1;

a₂) forming polyurethane prepolymer by reacting the polyurethane preadduct formed in step a₁) with 0.1 to 1.5 parts by weight of a low-molecular weight and anionically modifiable polyol component (A)(iii) containing one or more hydroxyl groups that are reactive with polyisocyanates and one or more inert carboxylic acid and/or sulfonic acid group(s) which can be partially or completely converted into carboxylate or sulfonate groups in the presence of bases or are already present in the form of carboxylate and/or sulfonate groups, having a molecular mass of 100 to 499 Daltons and with 0 to 8 parts by weight of a hydroxy functional component (A)(iv) containing two or more hydroxyl groups that are reactive with polyisocyanates and other hydrophilic groups that are inert towards polyisocyanates having a molecular mass of 500 to 5000 Daltons;

a₃) forming a multifunctional polyurethane oligomer or polymer by reacting the free isocyanate groups of the polyurethane prepolymer from step a₂) with 0.1 to 15 parts by weight of a multifunctional chain stopping component (D) containing three or more hydroxyl groups and/or primary and/or secondary amino groups that are reactive with isocyanate groups and having a molecular mass of 50 to 500 Daltons, one of the hydroxyl groups or one of the amino groups reacts with the polyurethane preadduct, the chain stopping component being in an amount that there is no unreacted polyol in a₃ in addition to the oligomer from step a₂ and wherein water dispersion of a₃ is achieved with conversion and hydrophilization to a salt of not more than about 20 meq/(100)g solid resin of ionic groups, and the hydroxyl and/or amino groups reducing an amount of anionic hydrophilization groups needed to disperse the binder in an aqueous media by at least 50% as compared to a binder not made according to a₁ through a₃;

a₄) reacting the multifunctional polyurethane oligomer or polymer from step a₃) with 0.1 to 1 parts by weight of a neutralization component (E) to partially or completely neutralize the acidic groups and to form neutralized polyurethane oligomer or polymer; and

a₅) dispersing the neutralized polyurethane oligomer or polymer from step a₄) in 40 to 60 parts by weight of water which also contains 0 to 50 parts by weight of a formulation component (F) to form a binder component, the neutralized polyurethane oligomer or polymer forming micelles having average particle size of from 10 nm to 300 nm in the water; and

b) reacting the binder component from step a₅) with a cross-linking component (H) in a ratio of 3;

1 to 5;

1, wherein the cross-linking component (H) comprises water-dispersible polyisocyanates containing aliphatically and/or cycloaliphatically and/or aromatically bound isocyanate groups which can contain 0 to 20 parts by weight of an organic solvent.

3. The polyurethane coating system as claimed in claim 2, further comprising:

a₆) reacting partially chain-terminated polyurethane oligomer or polymer from step a₅) with 0 to 15 parts by weight of a chain extending component (G) containing two or more primary and/or secondary amino groups that are reactive with isocyanate groups and having a molecular mass of 50 to 500 Daltons.

4. The polyurethane coating system as claimed in claim 2, wherein the higher-molecular weight polyol component (A)(i) comprises polyalkylene glycols, aliphatic or aromatic polyesters, polycaprolactones, polycarbonates, α

, ω

-polymethacrylatedioles, α

, ω

-dihydroxyalkylpoly- dimethylsiloxanes, hydroxyfunctional macro-monomers, hydroxyfunctional telechels, hydroxyfunctional epoxide resins having a molecular mass of 1000 to 3000 Dalton or suitable mixtures thereof.

5. The polyurethane coating system as claimed claim 2 wherein the component (A)(i) is linear or difunctional hydrophobically modified polyether polyols comprising saponification-resistant block copolymers having an ABA, BAB or (AB)_n structure in which A represents a polymer segment with hydrophobizing properties and B represents a polymer segment based on polypropylene oxide having an average molecular mass or 1000 to 3000 Daltons.

6. The polyurethane coating system as claimed in claim 2, wherein the component (A)(ii) is 1,4-butanediol.

7. The polyurethane coating system as claimed in claim 2, wherein the component (A)(iii) comprises a bishydroxyalkanecarboxylic acid and/or bishydroxysulfonic acid or alkali salts thereof having a molecular mass of 100 to 499 Daltons.

8. The polyurethane coating system as claimed in claim 7, wherein the bishydroxyalkanecarboxylic acid comprises 2-hydroxymethyl-2-methyl-3-hydroxypropionic acid or dimethylol-propionic acid.

9. The polyurethane coating system as claimed in claim 2, wherein the component (A)(iv) comprises reaction products of poly(ethylene oxide[-co/block/ran-propylene oxide])-monoalkyl ethers, a diisocyanate and diethanolamine.

10. The polyurethane coating system as claimed in claim 2, wherein the multi-functional chain-stopper component (D) comprises aliphatic of cycloaliphatic polyols and/or polyamines and/or amino-alcohols.

11. The polyurethane coating system as claimed in claim 10, wherein the multi-functional chain-stopper component (D) comprises diethanolamine and/or trimethylolpropane.

12. The polyurethane coating system as claimed in claim 2, wherein the formulation component (F) comprises antifoaming agents, deaerators, lubricating and flow-control additives, radiation hardening additives, dispersing additives, substrate wetting additives, hydrophobizing agents, rheology additives such as polyurethane thickeners, coalescing agents, dulling agents, bonding agents, antifreeze agents, antioxidants, UV stabilizers, bactericides, fungicides, other polymers and/or polymer dispersions as well as fillers, pigments, dulling agents or suitable combinations thereof.

13. The polyurethane coating system as claimed in claim 2, wherein the cross-linking component (H) comprises water-dispersible polyisocyanates containing aliphatically and/or cycloaliphatically and/or aromatically bound isocyanate groups which contain 0 to 20 parts by weight of an organic solvent.

14. The polyurethane coating system as claimed in claim 2 wherein the NCO/OH equivalent ratio of components (A) and (B) is adjusted to a value of 1.5:

1 to 2.25;

1.

15. The polyurethane coating system as claimed in claim 2, wherein the reactions of steps a_l) and a₂) are carried out in the presence of 0.01 to 1 weight % based on the components (A) and (B) of a conventional catalyst for polyaddition reactions on polyisocyanates.

16. The polyurethane coating system as claimed in claim 2, wherein the chain-stopper component (D) is added in such an amount that the degree of chain termination based on the free isocyanate groups of the polyurethane prepolymer comprising components (A) and (B) is 80 to 100 equivalent %.

17. The polyurethane coating system as claimed in claim 2, wherein the neutralization component (E) is added in such an amount that the degree of neutralization based on the free carboxylic acid and/or sulfonic acid groups of the polyurethane oligomer or polymer consisting of components (A), (B) and (D) is 70 to 100 equivalent %.

18. The polyurethane coating system as claimed in claim 17, wherein the degree of neutralization is 80 to 90 equivalent %.

19. The polyurethane coating system as claimed in claim 3, wherein the chain extending component (G) is added in such an amount that the degree of chain extension based on the free isocyanate groups of the polyurethane oligomer or polymer consisting of components (A), (B), (D) and (E) is 0 to 20 equivalent %.

20. The polyurethane coating system as claimed in claim 19, wherein the solids content of polyurethane oligomer or polymer comprising components (A), (B), (D), (E) and (G) is adjusted to 35 to 70 weight %, based on the total amount of the aqueous binder component consisting of components (A) to (E) and (G).

21. The polyurethane coating system as claimed in claim 20, wherein the solids content is adjusted to 45 to 55 weight %.

22. The polyurethane coating system as claimed in claim 20, wherein an average particle size of micelles of the aqueous binder component comprising components (A) to (E) and (G) is 10 to 300 nm.

23. The polyurethane coating system as claimed in claim 2, wherein the polyurethane oligomer or polymer consisting of the components (A), (B), (D), (E) and (G) has an average molecular mass of 1000 to 20,000 Daltons.

24. The polyurethane coating system as claimed in claim 2, wherein the NCO/(OH+NH₍₂₎-equivalent ratio of the isocyanate groups of the cross-linking component and the hydroxyl and/or amino groups of the binder component is adjusted to 1.1 to 1.6.

25. The polyurethane coating system as claimed in claim 24, wherein the NCO/(OH+NH₍₂₎₎-equivalent ratio is 1.2 to 1.4.

26. A method of producing the aqueous two-component polyurethane coating system of claim 2, comprising

a₁) reacting the components (A)(i), (A)(ii), (B) and (C) to form a polyurethane preadduct during which reacting the hydroxyl groups of components (A)(i) and (A)(ii) with the isocyanate groups of component (B);

a₂) reacting the polyurethane preadduct from reaction step a₁) with components (A)(iii) and (A)(iv) to form an anionically modifiable polyurethane prepolymer;

a₃) reacting the anionically modifiable polyurethane prepolymer from reaction step a₂) with component (D) to form a functionalized and anionically modifiable polyurethane oligomer or polyurethane polymer so that in each case only one reactive group of component (D) reacts with one isocyanate group of the polyurethane preadduct;

a₄) reacting the functionalized and anionically modifiable polyurethane oligomer or polyurethane polymer from reaction step a₃) which has two or more reactive groups per chain end and a total functionality of 4 with component (E) for partial or complete neutralization to form a binder component;

a₅) dispersing the functionalized and anionically modifiable polyurethane oligomer or polyurethane polymer from reaction step a₄) in water; and

b) reacting the binder component from reaction step a₅) with the modified cross-linking component (H), the cross-linking component (H) being added to the binder component, and obtaining a cross-linked, water proof and chemical resistant polyurethane coating system.

27. The method of claim 26, wherein in step a₅) the water also contains the component (F).

28. The method of claim 26, further comprising:

a₆) reacting the only partially chain-stopped, functionalized and anionically modified polyurethane oligomer or polyurethane polymer from step a₅) with component (G).

29. The method of claim 26, wherein steps a₄) and a₅) are combined in such a manner that component (E) is added to the water before dispersion.

30. The method of claim 26, wherein steps a₄) and a₅) are combined in such a manner that component (G) is added to the water before dispersion.

31. The method of claim 26, wherein steps a₁) and a₃) are carried out at a temperature of 60 to 120°

C.

32. The method of claim 31, wherein steps a₁) and a₃) are carried out at a temperature of 80 to 100°

C.

33. The method of claim 26, wherein step a₄) is carried out at a temperature of 40 to 65°

C.

34. The method of claim 33, wherein step a₄) is carried out at 50°

C.

35. The method of claim 26, wherein step b) is carried out at a temperature of 20 to 40°

C.

36. The method of claim 35, wherein step b) is carried out at a temperature of 20°

C.

37. A coating for surfaces, comprising the aqueous two-component polyurethane coating system of claim 2, wherein the coating is a formulated chemical-resistant and lightfast paint effective for coating surfaces selected from the group consisting of concrete, plaster, ceramics, clay, cement, glass, rubber, wood, derived timber products, plastic, metal, paper, composite materials, and leather.

38. Construction coating material comprising the aqueous two-component polyurethane coating system of claim 2, individually or in combination, wherein the material is used for coating indoor floors, balconies, parking decks and multi-story parking garages.

39. A coating for surfaces, comprising the aqueous two-component polyurethane coating system of claim 2, wherein the coating is an unformulated chemical-resistant and lightfast paint effective for coating surfaces selected from the group consisting of concrete, plaster, ceramics, clay, cement, glass, rubber, wood, derived timber products, plastic, metal, paper, composite materials, and leather.

40. The aqueous cross-linked two-component polyurethane coating system as recited in claim 2 wherein the hydroxyl and/or amino groups reduce the amount of anionic hydrophilization groups needed to disperse the binder in an aqueous media by 50% to 80% as compared to a binder not made according to a₁ through a₃.

41. The aqueous cross-linked two-component polyurethane coating system as recited in claim 2 wherein the hydroxyl and/or amino groups reduce the amount of anionic hydrophilization groups needed to disperse the binder in an aqueous media by 50% to 75% as compared to a binder not made according to a₁ through a₃.