Process for the production of an OEM base coat/clear top coat multi-layer coating

Patent metadata

Field	Value
Publication number	US-9688877-B2
Application number	US-201314390468-A
Country	US
Kind code	B2
Filing date	May 20, 2013
Priority date	Jul 5, 2012
Publication date	Jun 27, 2017
Grant date	Jun 27, 2017

Abstract

A process for the production of an OEM base coat/clear top coat multi-layer coating wherein a waterborne base coat composition is spray-applied by electrostatically-assisted high speed rotary atomization, wherein the waterborne base coat composition comprises binder solids comprising about 20 to about 100 wt. % of an aqueously dispersed polyurethane urea resin with a carboxyl number of about 10 to 50 mg KOH/g.

First claim

What is claimed is:

1. A process for the production of an OEM base coat/clear top coat multi-layer coating comprising the steps of:
(1) providing a substrate to be provided with an OEM base coat/clear top coat multi-layer coating,
(2) spray-applying a first waterborne base coat composition on said substrate by electrostatically-assisted high speed rotary atomization to form a base coat layer,
(2″) spray-applying a second waterborne base coat composition materially different from the first waterborne base coat on said base coat layer to form a color- and/or effect imparting coating layer,
(3) spray-applying a clear coat composition on the color- and/or effect imparting coating layer to form a clear top coat layer, and
(4) jointly curing the base coat, color- and/or effect imparting coating, and the clear top coat layers,
wherein the first waterborne base coat composition comprises water, pigment(s) and resin solids consisting of binder solids and, optionally, crosslinker solids,
wherein said binder solids consist of about 20 to about 100 wt. % of an aqueously dispersed polyurethane urea resin with a carboxyl number of about 10 to about 50 mg KOH/g and 0 to about 80 wt. % of other binders,
wherein the sum of the wt. % totals 100 wt. %,
wherein said aqueously dispersed polyurethane urea resin is made by a process comprising the steps of:
(i) producing a non-gelled polyurethane prepolymer with a free isocyanate group content of about 0.5 to about 4.5 wt. % by reacting at least one polyol, at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300, at least one polyhydroxycarboxylic acid which may or may not be neutralized with a tertiary amine, and at least one polyisocyanate, in the presence of at least one ketone and/or at least one other inert organic solvent,
(ii) if not already effected, neutralizing the carboxyl group(s) of the at least one polyhydroxycarboxylic acid with a tertiary amine before carrying out step (iii),
(iii) converting the so obtained ketone and/or other inert organic solvent solution of the polyurethane prepolymer into an aqueous dispersion by mixing with water, and
(iv) chain extending the polyurethane prepolymer by reacting the free isocyanate groups thereof with at least one compound having at least two amino groups capable of addition to isocyanate groups to form urea groups.

2. The process of claim 1 , wherein the at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300 is used in a proportion of about 0.02 to about 0.15 equivalents relative to the NCO provided by the at least one polyisocyanate employed in step (i).

3. The process of claim 1 , wherein the at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300 is an aliphatic monoalcohol compound with 1 to 18 carbon atoms.

4. The process of claim 3 , wherein the aliphatic monoalcohol compound with 1 to 18 carbon atoms is 1-butanol or butoxy ethanol.

5. The process of claim 1 , wherein the at least one polyhydroxycarboxylic acid is dimethylol propionic acid or dimethylol butyric acid.

6. The process of claim 1 , wherein step (i) is carried out with an NCO:total OH equivalent ratio of about 1.5:1 to about 1.05:1.

7. The process of claim 1 , wherein the polyurethane prepolymer formed in step (i) is linear.

8. The process of claim 1 , the second waterborne base coat composition is pneumatically spray-applied.

9. A process for the production of an OEM base coat/clear top coat multi-layer coating comprising the steps of:
(1) providing a substrate to be provided with an OEM base coat/clear top coat multi-layer coating,
(2) spray-applying a waterborne base coat composition on said substrate by electrostatically-assisted high speed rotary atomization to form a base coat layer,
(3) spray-applying a clear coat composition on the base coat layer to form a clear top coat layer, and
(4) jointly curing the base coat and the clear top coat layers,
wherein the waterborne base coat composition comprises water, pigment(s) and resin solids consisting of binder solids and, optionally, crosslinker solids,
wherein said binder solids consist of about 20 to about 100 wt. % of an aqueously dispersed polyurethane urea resin with a carboxyl number of about 10 to about 50 mg KOH/g and 0 to about 80 wt. % of other binders,
wherein the sum of the wt. % totals 100 wt. %,
wherein said aqueously dispersed polyurethane urea resin is made by a process comprising the steps of:
(i) producing a non-gelled polyurethane prepolymer with a free isocyanate group content of about 0.5 to about 4.5 wt. % by reacting at least one polyol, at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300, at least one polyhydroxycarboxylic acid which may or may not be neutralized with a tertiary amine, and at least one polyisocyanate, in the presence of at least one ketone and/or at least one other inert organic solvent,
(ii) if not already effected, neutralizing the carboxyl group(s) of the at least one polyhydroxycarboxylic acid with a tertiary amine before carrying out step (iii),
(iii) converting the so obtained ketone and/or other inert organic solvent solution of the polyurethane prepolymer into an aqueous dispersion by mixing with water, and
(iv) chain extending the polyurethane prepolymer by reacting the free isocyanate groups thereof with at least one compound having at least two amino groups capable of addition to isocyanate groups to form urea groups,

wherein the at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300 is used in a proportion of about 0.02 to about 0.15 equivalents relative to the NCO provided by the at least one polyisocyanate employed in step (i); wherein step (2) is followed by an additional step (2″) prior to step (3) being performed, wherein the waterborne base coat composition spray-applied in step (2) comprises a free polyisocyanate crosslinker, and wherein in step (2″) a waterborne base coat composition which is free of free polyisocyanate crosslinker is spray-applied to form a coating layer.

10. The process of claim 9 , wherein the waterborne base coat composition spray-applied in step (2″) has the same pigment composition like the waterborne base coat composition spray-applied in step (2).

11. The process of claim 1 , wherein the color- and/or effect imparting coating layer is transparent or semi-transparent.

12. A waterborne base coat composition comprising water, pigment(s) and resin solids consisting of binder solids and, optionally, crosslinker solids,
wherein said binder solids consist of about 20 to about 100 wt. % of an aqueously dispersed polyurethane urea resin with a carboxyl number of about 10 to about 50 mg KOH/g and 0 to about 80 wt. % of other binders,
wherein the sum of the wt. % totals 100 wt. %,
wherein said aqueously dispersed polyurethane urea resin is made by a process comprising the steps:
(i) producing a non-gelled polyurethane prepolymer with a free isocyanate group content of about 0.5 to about 4.5 wt. % by reacting at least one polyol, at least one compound having one alcoholic hydroxyl group and a molar mass of about 32 to about 300 and lacking other functional groups capable of reacting with the free isocyanate group content, at least one polyhydroxycarboxylic acid which may or may not be neutralized with a tertiary amine, and at least one polyisocyanate, in the presence of at least one ketone and/or at least one other inert organic solvent,
(ii) if not already effected, neutralizing the carboxyl group(s) of the at least one polyhydroxycarboxylic acid wit

Assignees

• Axalta Coating Systems Ip Co
• Axalta Coating Systems Ip Co

Inventors

• Flosbach Carmen
• Enkisch-Krug Charlotte
• Stoffel Petra

Classifications

• B05D1/00

  Processes for applying liquids or other fluent materials (B05D5/00, B05D7/00 take precedence) · CPC title

• B05D1/007

  using an electrostatic field (B05D1/02 - B05D1/16 take precedence) · CPC title

• C08G18/2825

  having at least 6 carbon atoms · CPC title

• B05D7/532

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

• B05D3/005

  Pretreatment for allowing a non-conductive substrate to be electrostatically coated · CPC title