Adhesion promoter for solventborne clearcoat materials

Patent metadata

Field	Value
Publication number	US-10344179-B2
Application number	US-201415104615-A
Country	US
Kind code	B2
Filing date	Dec 17, 2014
Priority date	Dec 17, 2013
Publication date	Jul 9, 2019
Grant date	Jul 9, 2019

Abstract

The present invention relates to a solventborne clearcoat material which comprises at least one additive preparable by reacting at least one alpha,omega-hydroxy-functionalized oligoester which has an OH number of 30 to 160 mg KOH/g, a theoretical carbon-carbon double bond content of 1 to 2.5 mmol/g, a number-average molecular weight of 1000 to 3000 g/mol, and a weight-average molecular weight of 2800 to 10 000 g/mol, and at least one alkoxysilane which possesses an OH-reactive functional group, the sum of the weight percentage fractions of all additives of the invention being 0.5 to 10 wt %, based on the total amount of the solventborne clearcoat material. The present invention further relates to a process for producing multicoat paint systems, and to multicoat paint systems producible by means of said process. The invention further relates to the use of the above-identified additive in solventborne clearcoat materials for the purpose of improving adhesion.

First claim

The invention claimed is:

1. A solventborne clearcoat material, comprising at least one additive prepared by reacting
(a) at least one alpha,omega-hydroxy-functionalized oligoester which possesses an OH number of 30 to 160 mg KOH/g, a theoretical carbon-carbon double bond content of 1 to 2.5 mmol/g, a number-average molecular weight of 1000 to 3000 g/mol, and a weight-average molecular weight of 2800 to 10000 g/mol, and
(b) at least one alkoxysilane of the structural formula (II)
A-R—Si(R′) x (OR″) 3−x

wherein
A is an OH-reactive functional group,
R is an aliphatic radical having 2 to 12 carbon atoms, a cycloaliphatic radical having 3 to 12 carbon atoms, an aromatic radical having 6 to 12 carbon atoms, or an araliphatic radical having 7 to 18 carbon atoms,
the radical R′ is selected from the group of C1 to C12 alkyl radical,
R″ is a methyl or ethyl radical, and
x is 0 to 2,

with the proviso that at least 90 mol % of all the OH groups of the alpha,omega-hydroxy-functionalized oligoester have been reacted with the OH-reactive functional group A, and, in addition,
the amount by weight of the at least one additive is 0.5 to 10 wt %, based on the total amount of the solventborne clearcoat material.

2. The solventborne clearcoat material of claim 1 , wherein the amount by weight of the at least one additive is 1.5 to 7.5 wt %, based on the total amount of the solventborne clearcoat material.

3. The solventborne clearcoat material of claim 1 , wherein the alpha,omega-hydroxy-functionalized oligoester possesses the following structural formula (I):

where
the radicals R1 independently of one another are selected from the group consisting of a linear alkylene radical and a cyclic alkylene radical,
the radicals R2 independently of one another are selected from the group consisting of an alkylene radical and an alkenylene radical, the ratio of alkylene to alkenylene radicals being selected specifically such that the alpha,omega-hydroxy-functionalized oligoester of the structural formula (I) possesses a theoretical carbon-carbon double bond content of 1 to 2.5 mmol/g, and
the index m is selected such that the number-average molecular weight of the alpha,omega-hydroxy-functionalized oligoester of the structural formula (I) is 1000 to 3000 g/mol.

4. The solventborne clearcoat material of claim 3 , wherein the radicals R 1 are linear alkylene radicals having 6 to 10 carbon atoms.

5. The solventborne clearcoat material of claim 3 , wherein the radicals R 2 are linear alkylene radicals having 4 to 8 carbon atoms or linear alkenylene radicals having 2 to 4 carbon atoms.

6. The solventborne clearcoat material of claim 3 , wherein the alkoxysilane possesses the general structural formula (II. 1)
OCN—R 1 —Si(R′) x (OR″) 3−x

wherein
R1 is a C2 to C12 alkylene radical, a C2 to C12 alkenylene radical, or a a C4 to C12 polyalkenylene radical,
the radical R′ is a C1 to C12 alkyl radical,
R″ is a methyl or ethyl radical, and
x is 0 to 2.

7. The solventborne clearcoat material of claim 6 , wherein R 1 is a C 2 to C 6 alkylene radical.

8. The solventborne clearcoat material of claim 7 , wherein x=0.

9. A process for producing a multicoat paint system on a substrate, the process comprising
(A) applying a basecoat material,
(B) applying the solventborne clearcoat material of claim 1 , and
(C) jointly curing the basecoat material and the clearcoat material.

10. A multicoat paint system produced by the process of claim 9 .

11. The process of claim 9 , wherein, atop the clearcoat film as per step (C),
i. a basecoat film is applied,
ii. a clearcoat film is applied, and
iii. the basecoat film and the clearcoat film are jointly cured.

12. A multicoat paint system produced by the process of claim 11 .

13. The process of claim 9 , wherein, atop the cured clearcoat film as per step (C), a sealant is applied.

14. A multicoat paint system produced by the process of claim 13 .

15. A process for improving the adhesion properties of a clearcoat, the process comprising formulating a solventborne clearcoat material with at least one additive prepared by reacting
(a) at least one alpha,omega-hydroxy-functionalized oligoester which possesses an OH number of 30 to 160 mg KOH/g, a theoretical carbon-carbon double bond content of 1 to 2.5 mmol/g, a number-average molecular weight of 1000 to 3000 g/mol, and a weight-average molecular weight of 2800 to 10000 g/mol, and
(b) at least one alkoxysilane of the structural formula (II)
A-R—Si(R′) x (OR″) 3−x

wherein
A is an OH-reactive functional group,
R is an aliphatic radical having 2 to 12 carbon atoms, a cycloaliphatic radical having 3 to 12 carbon atoms, an aromatic radical having 6 to 12 carbon atoms, or an araliphatic radical having 7 to 18 carbon atoms,
the radical R′ is a C1 to C12 alkyl radical,
R″ is a methyl or ethyl radical, and
x is 0 to 2,

with the proviso that at least 90 mol % of all the OH groups of the alpha,omega-hydroxy-functionalized oligoester have been reacted with the OH-reactive functional group A, and, in addition,
the amount by weight of the at least one additive is 0.5 to 10 wt %, based on the total amount of the solventborne clearcoat material.

Assignees

• Basf Coatings Gmbh

Inventors

• Andersen Audree
• Corten Cathrin
• Raka Fatmir
• Niemeier Manuela
• Freitag Nicole
• Boshe-Plois Stefanie
• Feigl Andreas
• Weiher Christian

Classifications

• C08K5/5419

  containing at least one Si—C bond · CPC title

• C08G18/718

  containing silicon · CPC title

• C08G18/68

  Unsaturated polyesters · CPC title

• B05D7/532

  the two layers being cured or baked together, i.e. wet on wet · CPC title

• C08G63/918

  Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation · CPC title