Coating agents having high scratch resistance and weathering stability
Disclosed are coating compositions comprising (a) at least one hydroxyl-containing compound (A), (b) at least one compound (B) having isocyanate groups, and (c) at least one catalyst (D) for the crosslinking of silane groups, said catalyst (D) comprising phosphorus. It is an aspect of the disclosed coating compositions that (i) one or more constituents of the coating composition contain hydrolyzable silane groups and (ii) the coating composition can be finally cured to a coating which has statistically distributed regions of an Si—O—Si network.
1. A coating composition comprising
(a) at least one hydroxyl-containing compound (A),
(b) at least one compound (B) having free and/or blocked isocyanate groups,
(c) at least one catalyst (D) for the crosslinking of silane groups, said catalyst (D) comprising phosphorus and nitrogen, and said catalyst (D) being blocked with a tertiary amine
where
(i) one or more constituents of the coating composition contain hydrolyzable silane groups and
(ii) the coating composition can be finally cured to a coating which has statistically distributed regions of an Si-O-Si network.
2. The coating composition of claim 1 , wherein the at least one catalyst (D) is selected from the group consisting of substituted phosphonic diesters, substituted diphosphonic diesters, substituted phosphoric monoesters, substituted phosphoric diesters and mixtures thereof.
3. The coating composition of claim 1 , wherein the catalyst (D) is selected from the group consisting of amine-blocked phosphoric acid ethylhexyl partial esters and amine-blocked phosphoric acid phenyl partial esters.
4. The coating composition of claim 1 , wherein one or more constituents of the coating composition comprise at least one or more, identical or different structural units of the formula (I)
—X—Si—R x G 3-x (I)
where
G =identical or different hydrolyzable groups, X =linear and/or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms, R″ =alkyl, cycloalkyl, aryl or aralkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
x =0 to 2.
5. A coating composition of claim 1 wherein one or more constituents of the coating composition comprise between 2.5 and 97.5 mol %, based on the entirety of structural units (II) and (III), of at least one structural unit of the formula (II)
—N(X—SiR″ x (OR′) 3-x ) n (X′—SiR″ y (OR′) 3-y ) m (II)
where
R′ =hydrogen, alkyl or cycloalkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
X, X′ =linear and/or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms,
R″ =alkyl, cycloalkyl, aryl or aralkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
n =0 to 2, m =0 to 2, m+n =2, and x =0 to 2, y =0 to 2, and
between 2.5 and 97.5 mol %, based on the entirety of structural units (II) and (III), of at least one structural unit of the formula (III)
—Z—(X—SiR″ x (OR′) 3-x ) (III),
where
Z =—NH—, —NR—, —0—, with
R =alkyl, cycloalkyl, aryl or aralkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
x =0 to 2, and
X, R′, R″ have the meaning given in formula (II).
6. The coating composition of claim 5 , wherein one or more constituents of the coating composition contain between 5 and 95 mol%, based on the entirety of the structural units (II) and (III), of at least one structural unit of the formula (II), and between 5 and 95 mol %, based on the entirety of the structural units (II) and (III), of at least one structural unit of the formula (III).
7. The coating composition of claim 6 , wherein the structural elements (II) and (III) are present in fractions of 2.5 to 97.5 mol %, based on the sum of the functional groups critical for crosslinking in the coating composition, formed from the fractions of the hydroxyl and isocyanate groups and from the fractions of the structural elements (II) and (III).
8. The coating composition of claim 7 , wherein the coating composition contains less than 6.5% by mass of Si of the structural units (II) and/or (III), based in each case on the solids content of the coating composition.
9. The coating composition of claim 5 , wherein the polyisocyanate (B) comprises the structural units (II) or (III).
10. The coating composition of claim 9 , wherein, the polyisocyanate (B) comprises a core polyisocyanate structure and in the polyisocyanate (B),
between 2.5 and 90 mol % of the isocyanate groups in the core polyisocyanate structure have undergone reaction to structural units (II) and
between 2.5 and 90 mol % of the isocyanate groups in the core polyisocyanate structure have undergone reaction to structural units (III)
and/or the total fraction of the isocyanate groups in the core polyisocyanate structure that have undergone reaction to structural units (II) and/or (III) is between 5 and 95 mol %.
11. The coating composition of claim 9 , wherein the polyisocyanate (B) comprises a core polyisocyanate structure selected from the group consisting of 1,6-hexamethylene diisocyanate, isophorone diisocyanate, and 4,4′-methylenedicyclohexyl diisocyanate, the biuret dimers of the aforementioned polyisocyanates, the isocyanurate trimers of the aforementioned polyisocyanates, and mixtures thereof.
12. The coating composition of claim 1 , wherein the polyol (A) comprises at least one poly(meth)acrylate polyol.
13. A multistage coating method which comprises applying a pigmented basecoat film to an uncoated or precoated substrate and thereafter applying a film of the coating composition of claim 1 .
14. The multistage coating method of claim 13 , wherein, following the application of the pigmented basecoat film, the applied basecoat material is first dried at temperatures from room temperature to 80° C. and, following the application of the coating composition of claim 1 , the system is cured at temperatures from 30 to 200° C. for a time of 1 min up to 10 h.
15. The coating composition of claim 1 that is a clearcoat material for automotive OEM finishing or automotive refinish.
16. The coating composition of claim 1 , wherein the at least one catalyst (D) is selected from the group consisting of acyclic phosphoric diesters, cyclic phosphoric diesters and mixtures thereof.
17. The coating composition of claim 1 , wherein the catalyst (D) is amine-blocked bis(ethylhexyl) phosphate.
18. A coating composition comprising:
(a) at least one hydroxyl-containing compound (A),
(b) at least one compound (B) having free and/or blocked isocyanate groups,
(c) at least one catalyst (D) for the crosslinking of silane groups, said catalyst (D) comprising phosphorus and nitrogen,
where
(i) one or more constituents of the coating composition contain hydrolyzable silane groups and
(ii) the coating composition can be finally cured to a coating which has statistically distributed regions of an Si-O-Si network
(iii) one or more constituents of the coating composition comprise between 2.5 and 97.5 mol %, based on the entirety of structural units (II) and (III), of at least one structural unit of the formula (II)
—N(X—SiR″ x (OR′) 3-x ) n (X′—SiR″ y (OR') 3-y ) m (II)
where
R′ =hydrogen, alkyl or cycloalkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
X, X′ =linear and/or branched alkylene or cycloalkylene radical having 1 to 20 carbon atoms,
R″ =alkyl, cycloalkyl, aryl or aralkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
n =0 to 2, m =0 to 2, m+n =2, and x =0 to 2, y =0 to 2, and
between 2.5 and 97.5 mol%, based on the entirety of structural units (II) and (III), of at least one structural unit of the formula (III)
—Z—(X—SiR″ x (OR′) 3-x ) (III),
where
Z =—NH—, —NR—, —0—, with
R =alkyl, cycloalkyl, aryl or aralkyl, in which a carbon chain may comprise nonadjacent oxygen, sulfur or NRa groups, with Ra =alkyl, cycloalkyl, aryl or aralkyl,
x =0 to 2, and
X, R′, R″ have the meaning given in formula (II).
19. A coating composition comprising:
(a) at least one hydroxyl-containing compound (A),
(b) at least one compound (B) having free and/or blocked isocyanate groups,
(c) at least one catalyst (D) for the crosslinking of silane groups, said catalyst (D) being an amine-blocked bis(ethylhexyl) phosphate
where
(i) one or more constituents of the coating composition contain hydrolyzable silane groups and
(ii) the coating composition can be finally cured to a coating which has statistically distributed regions of an Si—O—Si network.