COATING MATERIAL SYSTEM BASED ON Li/Bi CATALYSTS

Abstract

Disclosed herein is a coating material system containing (A) at least one polyhydroxy group-containing compound, (B) at least one polyisocyanate-containing compound, and (C) at least one catalyst comprising lithium (Li) and bismuth (Bi) as metal components and where the molar ratio of lithium to bismuth is at least 7:1 [mol/mol], in which i) components (A), (B), and (C) are present separately from one another, or ii) are mixed wholly or at least partly with one another. Methods for producing and using the coating material system are also disclosed herein.

Claims

1-18. (canceled).

19. A coating material system, comprising: (A) at least one polyhydroxy group-containing compound, (B) at least one polyisocyanate-containing compound, and (C) at least one catalyst comprising lithium (Li) and bismuth (Bi) as metal components and where the molar ratio of lithium to bismuth is at least 7:1 [mol/mol], wherein: i) components (A), (B), and (C) are present separately from one another, or ii) are mixed wholly or at least partly with one another.

20. The coating material system of claim 19, wherein the catalyst of component (C) has i) a molar ratio of lithium to bismuth of 7.5:1 to 12:1 [mol/mol], or ii) at least one further metal component.

21. The coating material system of claim 19, wherein: i) the polyhydroxy group-containing compound of component (A) is selected from the group consisting of the polyacrylate polyols, the polymethacrylate polyols, the polyester polyols, the polyurethane polyols or the polysiloxane polyols, or ii) the polyisocyanate-containing compound of component (B) is selected from the group consisting of 1,6-hexamethylene diisocyanate, isophorone diisocyanate, 4,4-methylene dicyclohexyl diisocyanate, the biuret dimers of the aforesaid diisocyanates, the iminooxadiazinediones of the aforesaid diisocyanates or the asymmetrical trimers of the aforesaid diisocyanates in the coating material system.

22. The coating material system of claim 19, wherein the acid number of the polyhydroxy group-containing compound of component (A) is not more than 9 mg KOH/g of the corresponding polyhydroxy group-containing compound.

23. The coating material system of claim 19, comprising at least one further component (D) to (J), selected from the group consisting of hydroxyl group-containing compounds (D), aminoplast resins or tris(alkoxycarbonylamino)triazines (E), coating additives (F), pigments (H), other fillers (I) or solvents (J), wherein i) the individual components (D) to (J) are present separately from one another, or ii) are mixed wholly or at least partly with one another or with components (A) to (C).

24. The coating material system of claim 19, wherein: i) the coating material system is not aqueous, or ii) components (A) or (B) each form a mixture with at least one solvent (J), but components (A) and (B) are present separately from one another, or iii) the catalyst of component (C) is present entirely or at least partly in at least one of the components (A) or (B) present separately from one another.

25. The coating material system of claim 19, wherein the catalyst of component (C) is present in the form of a salt.

26. The coating material system of claim 19, wherein the coating material system is present as a complete mixture of components (A), (B), and (C) and also of optionally present components (D) to (J).

27. A method for producing a coating material system of claim 26, wherein components (A), (B), and (C) and also optionally present components (D) to (J) are provided separately from one another and subsequently mixed with one another.

28. A method for producing a polyurethane by at least partial or complete curing of the coating material system of claim 26.

29. The method of claim 28, wherein the polyurethane forms a layer or coating or is at least part of a layer or coating.

30. The method of claim 28, wherein the polyurethane comprises at least one pigment (H) or wherein the polyurethane is applied in layer form to a basecoat film which optionally comprises at least one pigment (H), or to an optionally precoated substrate.

31. The method of claim 28, wherein the curing of the polyurethane takes place at temperatures of 20 to 80 C., the optional basecoat film having optionally been dried beforehand at temperatures of 20 C. to 80 C.

32. A coating material, comprising the coating material system of claim 19, wherein the coating material is adapted to function as a coating material in automotive finishing, for the repair of finishes, for automotive refinishing or for the coating of parts for installation in or on automobiles, of plastics substrates, or of commercial vehicles.

33. A method for producing a coating, comprising applying at least one coating material system of claim 19 to an optionally precoated substrate or to a basecoat film.

34. The method of claim 33, wherein the coating comprises a polyurethane which is obtained by at least partial or complete curing of the coating material system.

35. A method, comprising catalyzing a urethane reaction by contacting the coating material system of claim 19 with a catalyst comprising lithium (Li) and bismuth (Bi) as metal components, wherein: a molar ratio of lithium to bismuth is at least 7:1 [mol/mol], and the urethane reaction is adapted for the production of polyurethanes, for the production of a paint, for the repair of a paint finish, for automotive refinishing, or for the coating of parts for installation in or on automobiles, of plastics substrates, or of commercial vehicles.

36. A catalyst, comprising lithium (Li) and bismuth (Bi) as metal components, wherein a molar ratio of lithium to bismuth is at least 7:1 [mol/mol].

37. The coating material system of claim 20, wherein the catalyst of component (C) has i) a molar ration of lithium to bismuth of 8:1 to 10:1 [mol/mol], or ii) zinc (Zn) as the at least one further metal component.

38. The coating material system of claim 21, wherein the polyhydroxy group-containing compound of component (A) is selected from the group consisting of the polyacrylate polyols or the polymethacrylate polyols.

39. The coating material system of claim 22, wherein the acid number of the polyhydroxy group-containing compound of component (A) is not more than 7 mg KOH/g of the corresponding polyhydroxy group-containing compound.

40. The coating material system as claimed in claim 22, wherein the acid number of the polyhydroxy group-containing compound of component (A) is 0.5 to 5 mg KOH/g of the corresponding polyhydroxy group-containing compound.

41. The coating material system of claim 23, wherein the coating material system comprises at least one further component selected from the group consisting of hydroxyl group-containing compounds (D), coating additives (F), pigments (H) or solvents (J).

42. The coating material system of claim 24, wherein the catalyst of component (C) is present entirely or at least partly in component (A).

43. The coating material system of claim 25, wherein the catalyst of component (C) is present in the form of a Li salt or Bi salt with C.sub.6-C.sub.18 carboxylic acids as anion component of the respective salt.

44. The coating material system of claim 25, wherein the catalyst of component (C) is present as Bi octoate, Li octoate, Li or Bi salt of C.sub.10 neodecanoic acid or Li or Bi salt of C.sub.9 neononanoic acid.

45. A method for producing a coating material system of claim 27, wherein the mixing occurs at room temperature, with components (A) and (C) being mixed with one another beforehand or component (B) being added to component (A) or to a mixture comprising component (A).

46. A method for producing a polyurethane, comprising complete curing of the coating material system of claim 26.

47. The method of claim 29, wherein the layer or coating is a coating-material film.

48. The method of claim 28, wherein the curing of the polyurethane occurs at temperatures of 20 to 60 C.

49. A coating material formed by the method of claim 28, wherein the coating material is a clearcoat or a pigmented paint.

50. The method of claim 34, wherein the coating comprises a polyurethane which is obtained by complete curing of the coating material system.

Description

[0170] The invention is illustrated below with examples.

[0171] 1. Component A

[0172] Preparation of an Inventive Polyacrylate Polyol

[0173] A 4 1 stainless steel reactor in pressure design, equipped with two feed vessels, a reflux condenser, and a stirring member, is charged with 487 g of butyl acetate. One of the feed vessels is charged with a mixture of 479 g of styrene, 242.2 g of methyl methacrylate, 164 g of n-butyl acrylate, 298 g of butyl methacrylate, 33.4 g of methacrylic acid, and 763 g of hydroxypropyl methacrylate. The second feed vessel is charged with 198 g of tert-butyl per-2-ethylhexanoate with 86 g of butyl acetate. At a pressure of 3 bar absolute, the reactor charge is heated to 140 C. When the temperature is reached, the initiator feed is started; the overall feed time is 270 minutes. 5 minutes after the start of the initiator feed, the monomer feed is commenced, and is fed in over 240 minutes. After the end of both feeds, the batch is held at 140 C. for a further 60 minutes, after which it is cooled down and let down. The solids content of the resin solution is adjusted with methyl ethyl ketone to 65%1%.

[0174] The polyacrylate polyol thus synthesized (in the form of a solid resin) has an acid number of 14.1 mg KOH/g resin solids and a solids content of 64.0%. The viscosity of the resin solution is 3483 mPas, measured using a rotary viscometer (Brookfield CAP 2000, spindle 3, 2500 s.sup.1). The OH number works out at 150 mg KOH/g (resin solids). The molecular weight of the resin is Mn=2608 D and Mw=5990 D (determined by means of GPC/see below).

[0175] The solids content (solids) is measured as follows: on a metal lid with a diameter of about 6-8 cm, a sample of polyacrylate polyol in solid resin form is applied in an amount of 1 g to an analytical balance. Following addition of 1 ml of a suitable solvent (butyl acetate), the metal lid is dried in a forced air oven at 130 C. for 60 minutes. The residue which remains represents the solids content of the polyacrylate polyol in solid resin form. A duplicate determination is performed in each case.

[0176] The gel permeation chromatography (GPC) is carried out at 40 C. using a high-pressure liquid chromatography pump and a refractive index detector. The eluent used is tetrahydrofuran, with an elution rate of 1 ml/min. Calibration is performed using a poly-MMA standard. The number-average molecular weight Mn, the weight-average molecular weight Mw, and Mp are determined, with the polymolecularity index Mp being calculated from Mp=Mw/Mn.

[0177] 2. Curing Agent Solution, Corresponding to Component B

[0178] A mixture of 95 parts of HMDI trimer (NCO content 23.50.5%) with 5 parts of an IPDI trimer (NCO content 11.90.4%) is diluted to a solids content of 85% in a 1:1 mixture of butyl acetate and xylene.

[0179] 3. Diluent

[0180] 1:1 mixture of xylene/butyl acetate (solvent)

[0181] 4. Catalyst (Component C)

[0182] The metal contents reported in Table 2 (see section 7) are achieved by individual addition to component A of

[0183] i) a Bi octoate solution in octanoic acid (2-ethylhexanoic acid) with a metal content of 25% Bi,

[0184] ii) an Li octoate solution in octanoic acid (2-ethylhexanoic acid) with a metal content of 2% Li.

[0185] 5. Coating Material Formula

TABLE-US-00001 TABLE 1 C1 I1 I2 C2 I3 I4 C3 1 Component A 85.1 85.1 85.1 85.1 85.1 85.1 85.1 2 Ethyl 8.75 8.75 8.75 8.75 8.75 8.75 8.75 ethoxypropionate 3 Tinuvin 292 0.9 0.9 0.9 0.9 0.9 0.9 0.9 BASF SE 4 Hydroxyphenylalkylbenzotriazole 1.3 1.3 1.3 1.3 1.3 1.3 1.3 5 Bi octoate 25% Bi 0.251 0.251 0.251 0.418 0.418 0.418 0.418 7 Lithium octoate 0.693 0.788 1.05 1.155 1.312 1.75 0 2% Li 9 Component B 32 32 32 32 32 32 32 10 Diluent 32 32 32 32 32 32 32

[0186] The concentration figures are absolute amounts (expressed in parts) based on the overall coating material formulation.

[0187] Production of the Coating Materials

[0188] For the production of the coating materials, items 1-4 are weighed out together and mixed homogeneously. The catalyst solutions are added individually directly before the start of experimentation, and are each mixed homogeneously with stirring. Component B and diluent are then likewise added and stirred in homogeneously. The coating film is then produced within not more than 30 minutes after the mixing of the components (see section 7). Ethyl ethoxypropionate is a solvent; Tinuvin 292 and hydroxyphenylalkylbenzotriazole are light stabilizers.

[0189] 6. Print Test (Determination of Curing Time)

[0190] The coating film is drawn down using a 100 m doctor blade onto a glass plate. After drying at 60 C. for 18 minutes, the glass plate is placed on a commercial laboratory balance within 10 minutes following removal from the oven. Under thumb pressure, the film is then loaded for 20 s with a 2 kg weight. This test is repeated every 20 minutes. For a coating film which is obviously still soft or tacky, a waiting period is first observed until the coating film has reached sufficient freedom from tack and sufficient hardness. The overall experimentation time is about 6 hours. If marking is still apparent after this time, it is rated as >360 min.

[0191] The experiments are evaluated after a storage time of 24 hours. For this evaluation, the surface of the coating is washed with an aqueous surfactant solution (commercial washing-up liquid) and with a soft cloth, in order to eliminate grease marks. Measurement always takes place against a standard. The coating is considered satisfactory if there is no thumb print visible on the coating film. The results of the experiments are shown in Table 2. This test is a measure of the assembly strength of refinishes; that is, the earlier the coating film attains its assembly strength following forced drying, the earlier that assembly work (or disassembly work for masking) can be commenced on the refinished bodywork.

[0192] 7. Results

TABLE-US-00002 TABLE 2 Use of catalysts comprising lithium and bismuth as metal components; I1 to I4 are inventive and C1 to C3 are comparative examples. C1 I1 I2 C2 I3 I4 C3 Bi [mmol] 0.3 0.3 0.3 0.5 0.5 0.5 0.5 Li [mmol] 1.98 2.25 3.0 3.3 3.75 5.0 0 Ratio 1/6.6 1/7.5 1/10 1/6.6 1/7.5 1/10 Bi/Li (molar) Print test >360 240 220 320 280 260 >360 18 60 C. (min)

[0193] The examples according to Table 2 show that the coating materials of the invention with a catalyst, in which the molar ratio of lithium to bismuth is at least 7:1 [mol/mol], exhibit much shorter cure times than coating material systems using catalysts which do not have this ratio.