Coating agent compositions that are suitable for dip coating and that cure at low temperature

Patent metadata

Field	Value
Publication number	US-11401428-B2
Application number	US-201816633694-A
Country	US
Kind code	B2
Filing date	Jul 20, 2018
Priority date	Jul 26, 2017
Publication date	Aug 2, 2022
Grant date	Aug 2, 2022

Abstract

Aqueous coating compositions are provided. The aqueous compositions include at least one type of organic polymer particles having an average particle size of 10 to 1000 nm, including isocyanate-reactive polymers (A), one or more ketoxime- and/or pyrazole-blocked polyisocyanates (B) including at least one aromatic hydrocarbyl radical or at least one cycloaliphatic hydrocarbyl radical, at least one polyanionic polymer (C), at least one complex fluoride (D) selected from the group consisting of hexa- or tetrafluorides of metallic elements of groups IVb, Vb and VIb of the Periodic Table of the Elements, and at least one aminosilane (E), wherein the aqueous coating compositions have a pH of 3 to 5, and have a total solids content of 5% to 35% by weight. Also provided are processes for producing these aqueous coating compositions, processes for coating metal ion-releasing surfaces with the aqueous coating compositions, and coatings obtained therefrom.

First claim

The invention claimed is:

1. An aqueous coating composition comprising
at least one type of organic polymer particles having a Z-average particle size of 10 to 1000 nm, measured by means of dynamic light scattering, comprising isocyanate-reactive polymers (A),
one or more ketoxime- and/or pyrazole-blocked polyisocyanates (B), comprising at least one aromatic hydrocarbyl group or at least one cycloaliphatic hydrocarbyl group,
at least one polyanionic polymer (C),
at least one complex fluoride (D) selected from the group consisting of hexa- or tetrafluorides of the metallic elements of groups IVb, Vb and VIb of the Periodic Table of the Elements, and
at least one aminosilane (E) comprising a silyl group of the formula Si(OR 7 ) 3-i (R 8 ) i in which R 7 is an alkyl group having 1 to 4 carbon atoms or is an O═C—CH 3 group, R 8 is an alkyl group having 1 to 4 carbon atoms and i is 0 or 1,
wherein the aqueous coating composition
has a pH of 3 to 5, and
has a total solids content (1 g sample, 60 min, 125° C.) of 5% to 35% by weight.

2. The aqueous coating composition according to claim 1 , wherein the ketoxime- and/or pyrazole-blocked polyisocyanate(s) (B) is/are based on tolylene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate and/or dicyclohexylmethane diisocyanate.

3. The aqueous coating composition according to claim 1 , wherein the ketoxime- and/or pyrazole-blocked polyisocyanate(s) (B) comprise(s) polyethylene oxide chains and/or poly(ethylene oxide-propylene oxide) chains and/or an organic group comprising one or more sulfo groups, sulfonate groups, carboxyl groups and/or carboxylate groups.

4. The aqueous coating composition according to claim 1 , wherein the polyanionic polymer (C) is selected from the group consisting of (C.i) naturally occurring anionic polysaccharides, naturally occurring polymers comprising acidic amino acids, (C.ii) semisynthetic polyanionic polysaccharides and lignosulfonates and (C.iii) fully synthetic polyanionic polymers.

5. The aqueous coating composition according to claim 1 , wherein the polyanionic polymer (C) is selected from the group consisting of pectins, gellans, alginates and polyacrylic acids.

6. The aqueous coating composition according to claim 1 , wherein the complex fluoride(s) (D) is/are selected from the group consisting of hexa- or tetrafluorides of titanium, zirconium or hafnium.

7. The aqueous coating composition according to claim 1 , wherein the aminosilane (E) is an aminosilane of the general formula (VII)
H 2 N-L-Si(OR 7 ) 3-i (R 8 ) i    (VII)

in which L is a divalent organic connecting group;
R 7 is an alkyl group having 1 to 4 carbon atoms or is an O═C—CH 3 group;
R 8 is an alkyl group having 1 to 4 carbon atoms; and
i is 0 or 1.

8. The aqueous coating composition according to claim 1 , wherein
a content of the organic polymer particles comprising isocyanate-reactive polymers (A) is 3% to 25% by weight, based on a total weight of the aqueous coating composition; and/or
a content of polyanionic polymers (C) is 0.01% to 5.0% by weight, based on the total weight of the aqueous coating composition; and/or
an amount of the complex fluorides (D), based on a metal ion therein, is 1.1·10 −6 mol to 0.30 mol, in each case per liter of the aqueous coating composition; and/or
a content of the aminosilanes (E) is 0.0005% to 1.0% by weight, based on the total weight of the aqueous coating composition.

9. The aqueous coating composition according to claim 1 , wherein a molar ratio of blocked NCO groups of the ketoxime- and/or pyrazole-blocked polyisocyanates (B) to the isocyanate-reactive groups of the polymers (A) is between 0.5:1 and 2.0:1.

10. The aqueous coating composition according to claim 1 , wherein a content of organic solvents is 0% to 15% by weight, based on the total weight of the aqueous coating composition.

11. A process for producing an aqueous coating composition as defined in claim 1 , which comprises:
either
(i) mixing the ketoxime- and/or pyrazole-blocked polyisocyanate(s) (B), with or without use of an external emulsifier, with a dispersion of the organic polymer particles that have a Z-average particle size of 10 to 1000 nm, measured by means of dynamic light scattering, and comprise one or more isocyanate-reactive polymers (A); or
(ii) preparing a dispersion of the organic polymer particles that have a Z-average particle size of 10 to 1000 nm, measured by means of dynamic light scattering, and comprise one or more isocyanate-reactive polymers (A) in the presence of the ketoxime- and/or pyrazole-blocked polyisocyanate(s) (B);
and which further comprises
(iii) mixing the polyanionic polymer(s) (C), the complex fluoride(s) (D) and the aminosilane(s) (E) into the mixture prepared in step (i) or the dispersion prepared in step (ii), either during or after preparation of the mixture in step (i) or during or after preparation of the dispersion in step (ii); and
(iv) subsequently adjusting the pH of the mixture formed in step (iii) to a value of 3 to 5.

12. A process for coating a metal ion-releasing surface of a substrate, comprising the steps of:
I. providing a substrate having a metal ion-releasing surface,
II. contacting the metal ion-releasing surface with an aqueous coating composition according to claim 1 to form an organic coating,
III. optionally rinsing the organic coating and
IV. optionally drying the organic coating at a temperature of 10 to 120° C. within a period of 1 to 40 min; and curing the organic coating at a peak metal temperature of 120 to 200° C. within a period of 5 to 50 min; or
V. optionally drying the organic coating and coating with a further aqueous coating composition according to claim 1 and then drying the coating formed in step V or both coatings;
and curing the two coatings together at a peak metal temperature of 120 to 200° C. within a period of 5 to 50 min.

13. The process for coating a metal ion-releasing surface of a substrate according to claim 12 , wherein the substrate is selected from
a. metallic substrates, comprising metals and/or alloys, and metals and/or alloys and/or nonmetallic substrates that have been coated with metals and/or alloys; and
b. nonmetallic substrates, comprising an underlying substrate coated with organic coatings and/or nonmetallic inorganic coatings, where metal ions have been incorporated into the coatings or metal ions released by the underlying substrate can diffuse through the coatings to the surface.

14. The process for coating a metal ion-releasing surface of a substrate according to claim 12 , wherein said substrate, prior to performance of step II, is subjected to a surface pretreatment comprising one or more of the following measures:
removing surface impurities;
activating the surface for the coating in step II; and/or
applying one or more corrosion-inhibiting and/or adhesion-promoting and/or metal ion-releasing layers.

15. A coating obtainable by the process according to claim 12 .

Assignees

• Chemetall Gmbh

Inventors

• Frenkel Aliaksandr
• Eilinghoff Ron
• Droll Martin

Classifications

• C08G18/6484

  Polysaccharides and derivatives thereof · CPC title

• C09D7/63

  organic · CPC title

• C09D5/082

  characterised by the anti-corrosive pigment · CPC title

• C08G18/0804

  Manufacture of polymers containing ionic or ionogenic groups · CPC title

• C08G18/8077

  Oximes · CPC title