Integrated Dual-Cure Coating Material System and Use Thereof for the Internal and External Coating of Complex Shaped Three-Dimensional Substrates

Abstract
An integrated dual-cure coating material system which comprises two dual-cure multicomponent systems (A) and (B) which are composed predominantly or wholly of the same constituents and comprise in each case two components stored separately from one another,
Description
EXAMPLES
Example 1
The Preparation of Integrated Dual-Cure Coating Material Systems
The Dual-Cure Two-Component Systems (A1) and (A2)

To prepare the integrated dual-cure coating material systems for producing integrated internal and external paint systems (B/A) on automobile bodies first of all the dual-cure two-component systems (A1) and (A2) listed in Table 1 were prepared by mixing the constituents to their components (I) and (II) and homogenizing the resulting mixtures (I) and (II) in the absence of UV radiation. The respective components (I) and (II) were stored separately from one another prior to their use.









TABLE 1







The physical composition of the dual-cure two-


component systems (A1) and (A2)









Constituent
(A1)
(A2)












Component (I):




Methacrylate copolymer (solids:
39.9
39.9


65% by weight; hydroxyl number: 175 mg KOH/g;


glass transition temperature: −21° C.)


Rheological assistant (SCA) based on urea
17.1
17.1


as in Preparation Example 3, page 11 lines


41 to 51, DE 102 04 114 A 1 (solids:


59% by weight)


Aerosil ® paste (solids: 28.47% by weight)
3.3
3.3


Dipentaerythrityl pentaacrylate (solids:
22.8
22.8


100% by weight)


Tinuvin ® 292 (commercial light stabilizer
1.1
1.1


from Ciba Specialty Chemicals; solids:


100% by weight)


Tinuvin ® 400 (commercial light stabilizer
1.1
1.1


from Ciba Specialty Chemicals; solids:


85% by weight)


Byk ® 358 (commercial coatings additive
0.9
0.9


from Byk Chemie; solids: 52% by weight)


Irgacure ® 184 (commercial photoinitiator
2.2
2.2


from Ciba Specialty Chemicals; solids:


50% by weight)


Lucirin ® TPO (commercial photoinitiator
1.1
1.1


from BASF Aktiengesellschaft; solids:


10% by weight)


Methoxypropanol
3
3


Butyl diglycol acetate
2
2


Butyl acetate
5.5
5.5


Component (II):


Isocyanato acrylate Roskydal ® UA VPLS 2337
55.02
48.1


from Bayer AG (basis: trimeric


hexamethylene diisocyanate; isocyanate


equivalent weight: 329 g; solids:


100% by weight)


Isocyanato acrylate Roskydal ® UA VP FWO
13.77
22.3


3003-77 from Bayer AG based on


the trimer of isophorone diisocyanate


(solids: 70.5% by weight; isocyanate


equivalent weight: 609 g)


Polyisocyanate based on isophorone diisocyanate
9.79
12.8


(Desmodur ® N 3300 from Bayer AG)


Butyl acetate 98/100
21.42
16.8









The Dual-Cure Two-Component Systems (B1) and (B5)

To prepare the integrated dual-cure coating material systems for producing integrated internal and external paint systems (B/A) on automobile bodies first of all the dual-cure two-component systems (B1) to (B5) listed in Table 2 were prepared by mixing the constituents to their components (I) and (II) and homogenizing the resulting mixtures (I) and (II) in the absence of UV radiation. The respective components (I) and (II) were stored separately from one another prior to their use.









TABLE 2







The physical composition of the dual-cure two-


component systems (B1) to (B5)












Constituent
(B1)
(B2)
 (B3)
(B4)
 (B5)










Component (I):












Methacrylate copolymera)


58.7




Methacrylate copolymerb)
39.9
39.9

38.7
38.7


Rheological assistant (SCA)c)
17.1
17.1
17.1
16.6
16.6


Aerosil ® pasted)
3.3
3.3
3.3
3.2
3.2


Dipentaerythrityl pentaacrylatee)
22.8
22.8
4.7
22.1
221


Tinuvin ® 292f)
1.1
1.1
1.1
1.1
1.1


Tinuvin ® 400g)
1.1
1.1
1.1
1.1
1.1


Byk ® 358h)
0.9
0.9
0.9
0.9
0.9


Irgacure ® 184i)
2.2
2.2
2.2
2.1
2.1


Lucirin ® TPOj)
5.5
5.5
5.5
5.3
5.3


Methoxypropanol
3
3
3
2.9



Butyl diglycol acetate
2
2
2
1.9
8.9


Butyl acetate
1.1
1.1
0.4
4.1








Component (II):












Isocyanato acrylatek)

9.2
9.2
9.2
9.2


Isocyanato acrylatel)
8.3
67.9
67.9
67.9
67.9


Polyisocyanatem)
5.9
7.2
7.2
7.2
7.2


Isocyanato acrylaten)
73






Butyl acetate 98/100
12.8
15.7
15.7
15.7
15.7






a)solids: 65% by weight; hydroxyl number: 175 mg KOH/g; glass transition temperature: −21° C.;




b)solids: 65% by weight; hydroxyl number: 175 mg KOH/g; glass transition temperature: +11° C.;




c)urea-based SCA as per Preparation Example 3, page 11 lines 41 to 51, of DE 102 04 114 A 1 (solids: 59% by weight);




d)solids: 28.47% by weight;




e)solids: 100% by weight;




f)commercial light stabilizer from Ciba Specialty Chemicals; solids: 100% by weight;




g)commercial light stabilizer from Ciba Specialty Chemicals; solids: 85% by weight;




h)commercial coatings additive from Byk Chemie; solids: 52% by weight;




i)commercial photoinitiator from Ciba Specialty Chemicals; solids: 50% by weight;




j)commercial photoinitiator from BASF Aktiengesellschaft; solids: 10% by weight;




k)Roskydal ® UA VPLS 2337 from Bayer AG (basis: trimeric hexamethylene diisocyanate; isocyanate group content: 12% by weight; solids: 100% by weight);




l)Roskydal ® UA VP FWO 3003-77 from Bayer AG, based on the trimer of isophorone diisocyanate (solids: 70.5% by weight; isocyanate group content: 6.7% by weight);




m)polyisocyanate based on isophorone diisocyanate (Desmodur ® N 3300 from Bayer AG);




n)Isocyanato acrylate based on 4,4′-dicyclohexylmethane diisocyanate (Desmodur ® W from Bayer AG) and 4-hydroxybutyl acrylate (solids: 70% by weight; isocyanate equivalent weight 724 g).







The Integrated Dual-Cure Coating Material Systems

Each of the above-described dual-cure multicomponent systems (A1) or (A2) was combinable with each of the above-described dual-cure multicomponent systems (B1), (B2), (B3), (B4) or (B5) to form an integrated dual-cure coating material system, giving a total of 10 such systems.


Example 2
The Coating of Automobile Bodies with Multicoat Effect Paint Systems Comprising Clearcoat Systems Produced Using the Integrated Dual-Cure Coating Material Systems
General Experimental Instructions

For the internal painting of automobile bodies beneath the trunk lid and the engine hood and in the area of the doorsills, trunk and insides of the doors and windows the dual-cure coating materials (B1) to (B5) were prepared shortly before application from the above-described dual-cure multicomponent systems (B1) to (B5) (cf. Example 1, Table 2) by mixing the respective components (I) and (II) in the following (I)/(II) mixing ratios (% by weight): (B1): 100/111; (B2): 100/111; (B3): 100/91; (B4): 100/89; (B5): 100/89.


For the external paint systems of automobile bodies the dual-cure coating materials (A1) and (A2) were prepared shortly before application from the above-described dual-cure two-component systems (A1) and (A2) (cf. Example 1, Table 1) by mixing the respective components (I) and (II) in the following (I)/(ll) mixing ratios (% by weight): (A1): 100/67; (A2): 100/65.


Automobile bodies which have been coated with a conventional electrocoat and a conventional primer-surfacer coat were coated with a commercially customary aqueous basecoat material comprising aluminum effect pigments. The aqueous basecoat films were briefly flashed off at room temperature and dried at 80° C. for 10 minutes. The wet film thicknesses were chosen so as to give film thicknesses of 12 to 15 μm after drying and curing.


The aqueous basecoat film in the interior of five automobile bodies was coated wet on wet with one each of the dual-cure coating materials (B1) to (B5), and the aqueous basecoat film on the outside was coated wet on wet with the dual-cure coating material (A1). The wet film thicknesses of the clearcoat films were set so as to give film thicknesses of 40 to 45 μm after curing.


The aqueous basecoat film in the interior of five automobile bodies was coated wet on wet with one each of the dual-cure coating materials (B1) to (B5), and the aqueous basecoat film on the outside was coated wet on wet with the dual-cure coating material (A2). The wet film thicknesses of the clearcoat films were set so as to give film thicknesses of 40 to 45 μm after curing.


The aqueous basecoat films and clearcoat films of the 10 automobile bodies were predried jointly at room temperature for 5 minutes and at 80° C. for 10 minutes, exposed to a UV radiation dose of 1500 mJ/cm2 and subsequently cured at 140° C. for 20 minutes.


The resulting internal paint systems (B) were hard and scratch-resistant, allowing installation of the further components of the automobile without any problems. The resulting external paint systems (A) were highly scratch-resistant and hard. Both paint systems had outstanding optical properties and very high light stability and chemical, water, condensation, weather and etch resistance. Their capacity for overcoating was outstanding. In particular, however, there were no longer any paint defects in the areas where the internal (B) and external (A) paint systems overlapped.

Claims
  • 1. An integrated dual-cure coating material system comprising: at least one dual-cure multicomponent systems (A) andat least one dual-cure multicomponent system (B),wherein the dual-cure multicomponent systems (A) and (B) are composed predominantly or wholly of the same constituents and comprise in each case at least a first components (I) and a second component (II) stored separately from one another,wherein the first component (I) comprises (i.1) isocyanate-reactive functional groups, and(i.2) reactive functional groups comprising at least one bond which can be activated with actinic radiation, andat least one of(i.3) flexibilizing structural units, which when parts of a three dimensional networks lowers glass transition temperature Tg, of the three dimensional network,(i.4) hardening structural units, which as part of a three-dimensional networks raises a glass transition temperature Tg of the three dimensional network, and mixtures thereof,and the second component (II) comprises (ii.1) free isocyanate groups,(ii.2) reactive functional groups comprising at least one bond which can be activated with actinic radiation, andat least one of (ii.3) flexibilizing structural units which as parts of a three-dimensional networks lowers a glass transition temperature Tg of the three dimensional network,(ii.4) hardening structural units which as parts of a three-dimensional networks raises a glass transition temperature Tg of the three dimensional network, and mixtures thereof,wherein the dual-cure multicomponent system (B) comprises at least one of (a)a lower quantity of reactive functional groups containing at least one bond which can be activated with actinic radiation as compared to dual-cure multicomponent system (A), (b)a higher quantity of hardening structural units as compared to dual-cure multicomponent system (A), or a mixture thereof.
  • 2. The integrated dual-cure coating system of claim 1, comprising two dual-cure multicomponent systems (A) and (B).
  • 3. The integrated dual-cure coating system of claim 1, comprising at least one dual-cure two-component system (A).
  • 4. The integrated dual-cure coating system of claims 1, comprising at least one dual-cure two-component system (B).
  • 5. The integrated dual-cure coating system of claim 1, wherein the dual-cure multicomponent systems (A) and (B) differ physically from one another in not more than two constituents.
  • 6. The integrated dual-cure coating system of claim 1, wherein components (I) comprises at least one oligomeric and/or polymeric binder containing isocyanate reactive functional groups (i.1).
  • 7. The integrated dual-cure coating system of claim 1, wherein components (I) comprises at least one low molecular mass and/or oligomeric constituent containing at least one reactive functional group.
  • 8. The integrated dual-cure coating system of claim 1, wherein components (II) comprises at least one constituent comprising at least one free isocyanate group and at least one reactive functional group comprising at least one bond which can be activated with actinic radiation.
  • 9. A method of internally and externally coating a three-dimensional substrates of complex shape, the method comprising applying the integrated dual coating system of claim 1 to the three-dimensional substrate of complex shape.
  • 10. The method of claim 9, wherein the three-dimensional substrate is at least one surface of an automobile body.
  • 11. A process for internally and externally coating a three-dimensional substrate of complex shape, the process comprising: (1) preparing at least one dual-cure material (A) and at least one dual-cure coating material (B) by mixing in each case at least one component (I) and at least one component (II) together to provide a mixture, and homogenizing the resulting mixture,(2) coating an outside of the three-dimensional substrate with the dual cure coating material (A) and an inside of the three-dimensional substrate with the dual-cure coating material (B), and(3) curing the resulting coatings (A) and (B) thermally and with actinic radiation to give the integrated internal and external coating (B/A).
Priority Claims (1)
Number Date Country Kind
10 2004 023 423.6 May 2004 DE national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/EP05/52385 5/19/2005 WO 00 11/16/2006