Aqueous dip-coating composition for electroconductive substrates, comprising bismuth and a phosphorus-containing, amine-blocked compound

Patent metadata

Field	Value
Publication number	US-2016369114-A1
Application number	US-201315103118-A
Country	US
Kind code	A1
Filing date	Dec 10, 2013
Priority date	Dec 10, 2013
Publication date	Dec 22, 2016
Grant date	—

Abstract

The present invention relates to an aqueous coating composition (A) comprising at least one cathodically depositable binder (A1) and optionally at least one crosslinking agent (A2), for at least partly coating an electrically conductive substrate with an electrocoat material, where (A) comprises a total amount of at least 30 ppm of bismuth, based on the total weight of (A), and additionally at least one phosphorus-containing compound (P) blocked with at least one amine of the general formula (I), to the use of (A) for at least partly coating an electrically conductive substrate with an electrocoat material, to a corresponding coating method, and to an at least partly coated substrate obtainable by this method.

First claim

1 . An aqueous coating composition (A), comprising
(A1)) at least one cathodically depositable binder; and (A2) optionally at least one crosslinking agent,
for at least partly coating an electrically conductive substrate with an electrocoat material,
wherein:
the coating composition (A) comprises a total amount of at least 30 ppm of bismuth, based on a total weight of the coating composition (A);
the coating composition (A) comprises at least one phosphorus-containing compound (P) blocked with at least one amine of the general formula (I);

R 1 and R 2 each independently of one another are a C 1-18 aliphatic radical, are a C 3-12 cycloaliphatic radical, are a C 3-12 cycloaliphatic radical bridged via a C 1-10 aliphatic group, or are an aryl or heteroaryl radical bridged via a C 1-10 aliphatic group; and
R 3 is H, a C 1-18 aliphatic radical, a C 3-12 cycloaliphatic radical, a C 3-12 cycloaliphatic radical bridged via a C 1-10 aliphatic group, or an aryl or heteroaryl radical bridged via a C 1-10 aliphatic group.

2 . The coating composition (A) of wherein the coating composition (A) has a pH ranging from 4.0 to 6.5.

3 . The coating composition (A) of claim 1 , comprising at least one phosphorus-containing compound (P), blocked with at least one amine of the general formula (1), in an amount of 0.05 to 5 wt %, based on the total weight of the coating composition (A).

4 . The coating composition (A) of claim 1 , wherein at least one of the radicals R 1 , R 2 , and R 3 is a C 1-18 aliphatic radical.

5 . The coating composition (A) of claim 1 , wherein at least one of the radicals R 1 , R 2 , and R 3 is a C 3-18 alkyl radical.

6 . The coating composition (A) of claim 1 , wherein R 3 is a C 1-18 aliphatic radical or is an aryl or heteroaryl radical bridged via a C 1-10 aliphatic group.

7 . The coating composition (A) of claim 1 , wherein the phosphorus-containing compound (P) is selected from the group consisting of a phosphonic diester, a diphosphonic diester, a phosphoric monoester, a phosphoric diester, anions thereof and mixtures thereof.

8 . The coating composition (A) of claim 1 , wherein:
the phosphorus-containing compound (P) is a compound of the general formula (II) below or an anion thereof;

R 4 and R 5 each independently of one another are selected from the group consisting of an unsubstituted (hetero)alkyl radical comprising 1 to 20 carbon atoms and optionally 1 to 4 heteroatoms selected from the group consisting of N, NH, N(C 1-6 alkyl), O, and S, an unsubstituted (hetero)cycloalkyl radical comprising 3 to 20 carbon atoms and optionally 1 to 4 heteroatoms selected from the group consisting of N, NH, N(C 1-6 alkyl), O, and S, and an unsubstituted (hetero)aryl radical comprising 5 to 20 carbon atoms and optionally 1 to 4 heteroatoms selected from the group consisting of N, NH, N(C 1-6 alkyl), O, and S; and
one of the radicals R 4 and R 5 , or both radicals R 4 and R 5 , may additionally also be hydrogen.

9 . The coating composition (A) of claim 1 , wherein the bismuth present in the coating composition (A) is present in a form in which it is in solution (A3) and/or not in solution (A4) in the coating composition (A).

10 . The coating composition (A) of claim 1 , wherein at least part of the total amount of bismuth present in the coating composition (A) is present in a form (A3) in which it is in solution in the coating composition (A).

11 . The coating composition (A) of claim 1 , wherein the total amount of bismuth present in the coating composition (A) is in a range from at least 30 ppm to 20 000 ppm.

12 . The coating composition (A) claim 1 , wherein the coating composition (A) comprises a total amount of at least 130 ppm of bismuth, based on the total weight of the coating composition (A), including
(A3) at least 100 ppm of bismuth, optionally at least 130 ppm of bismuth, based on the total weight of the coating composition (A), in a form in which it is in solution in the coating composition (A), or (A3) at least 30 ppm of bismuth, based on the total weight of the coating composition (A), in a form in which it is in solution in the coating composition (A), and (A4) at least 100 ppm of bismuth, based on the total weight of the coating composition (A), in a form in which it is not in solution in the coating composition (A).

13 . The coating composition (A) of claim 1 , wherein the coating composition (A) further comprises
(A5) at least one at least bidentate complexing agent suitable for complexing bismuth.

14 . The coating composition (A) of claim 13 , wherein the at least one complexing agent (A5) is present in the aqueous coating composition (A) in a fraction of at least 5 mol %, based on the total amount of bismuth present in the coating composition (A).

15 . The coating composition (A) of claim 1 , wherein the binder (A1) is a polymeric resin which has at least partly protonated tertiary amino groups, and the crosslinking agent (A2) present optionally is a blocked isocyanate.

16 . The coating composition (A) of claim 15 , wherein the tertiary amino groups each independently of one another have at least two C 1-3 alkyl groups each at least singly substituted by a hydroxyl group.

17 . A method, comprising at least partly coating an electrically conductive substrate with the aqueous coating composition (A) of claim 1 in the form of the electrocoat material.

18 . A method for at least partly coating an electrically conductive substrate with an electrocoat material, the method comprising:
(1) contacting the electrically conductive substrate, connected as cathode, with the aqueous coating composition (A) of claim 1 .

19 . The method of claim 18 , wherein step (1) is carried out in at least two successive stages (1a) and (1b):
(1a) at an applied voltage in a range from 1 to 50 V, which is applied over a duration of at least 5 seconds, and (1b) at an applied voltage in a range from 50 to 400 V, with the proviso that the voltage applied in stage (1b) is greater by at least 10 V than the voltage applied in stage (1a).

20 . The method of claim 19 , the voltage applied in stage (1a) is applied over a duration in a range from at least 5 to 300 seconds.

21 . The method of claim 19 , wherein the voltage applied in stage (1b) in the range from 50 to 400 V takes place in a time interval of 0 to 300 seconds after implementation of stage (1a) and is maintained for a period in the range from 10 to 300 seconds at a value within the stated voltage range of 50 to 400 V.

22 . An electrically conductive substrate coated at least partly with the aqueous coating composition (A) of claim 1 .

23 . The electrically conductive substrate of claim 22 , wherein the substrate has at least one surface of aluminum.

24 . An article or component produced from at east one electrically conductive substrate of claim 20 .

Assignees

• Basf Coatings Gmbh
• Henkel Ag & Co Kgaa

Inventors

• Holtschulte Sabine
• Niegemeier Andreas
• Stoll Dominik

Classifications

• C23C18/1254

  Sol or sol-gel processing · CPC title

• C09D5/4488

  Cathodic paints (C09D5/4403 - C09D5/4476 take precedence) · CPC title

• C25D13/06

  with polymers {(not used, see C09D5/44)} · CPC title

• C25D9/02

  with organic materials · CPC title

• C09D5/443

  Polyepoxides · CPC title