CA2595366A1 - Coating compositions and methods of applying the same - Google Patents

Coating compositions and methods of applying the same Download PDF

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Publication number
CA2595366A1
CA2595366A1 CA002595366A CA2595366A CA2595366A1 CA 2595366 A1 CA2595366 A1 CA 2595366A1 CA 002595366 A CA002595366 A CA 002595366A CA 2595366 A CA2595366 A CA 2595366A CA 2595366 A1 CA2595366 A1 CA 2595366A1
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Prior art keywords
reactive component
coating composition
coating
layer
reactive
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Granted
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CA002595366A
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French (fr)
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CA2595366C (en
Inventor
Dennis Lee Havlin Jr.
Mark Edward Nichols
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Ford Motor Co
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Ford Motor Co
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/36Successively applying liquids or other fluent materials, e.g. without intermediate treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/14Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to metal, e.g. car bodies
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D7/00Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
    • B05D7/50Multilayers
    • B05D7/52Two layers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/16Catalysts
    • C08G18/18Catalysts containing secondary or tertiary amines or salts thereof

Abstract

One aspect of the present invention is a coating system for use in a wet on wet coating application process. The coating system includes a first coating composition, a second coating composition, and a boundary layer. The first coating composition includes a first bulk polymer resin and a first reactive component selected from the group consisting of a part A and a part B reactive component. The second coating composition includes a second bulk polymer resin and a second reactive component comprised of the other reactive component of the part A and the part B reactive component group. The boundary is formed upon applying a first layer of the first coating composition to a second layer of the second coating composition. The boundary layer includes the reaction product of the part A and the part B reactive component and is situated between the first layer and the second layer.

Description

COATING COMPOSITIONS AND METHODS OF APPLYING THE SAME
CROSS-REFERENCE TO RELATED APPLICATION
This application claims the benefit of U.S.
Provisional Application Serial No. 60/821,174, filed August
2, 2006.

BACKGROUND
1. Technical Field One aspect of the present invention relates to coating compositions and another aspect of the present invention relates to applying coating compositions to substrates.

2. Background Art Many known paint application systems include the application and curing of multiple layers of coatings, which result in the original finish to the exterior surfaces of consumer products, including, but not limited to, automotive vehicles. As one example, wet on wet paint application systems involve the application of a subsequent coating to a substantially uncured previously applied coating. The two substantially uncured coatings are then jointly cured by a curing process, which may involve a curing oven.
One proposed wet on wet paint application system includes the sequential application of multiple coating compositions, including an electrocoat (ecoat), a primer coat, a basecoat and a clearcoat. The ecoat is applied to a substrate (for example, an automotive vehicle panel) and is subsequently cured. Furthermore, the wet on wet system includes applying the primer coat to the cured ecoat, curing the primer coat, subsequently applying the basecoat to the cured primer coat, and subsequently applying the clearcoat to the uncured basecoat. The adjacent uncured coating layers, i.e., the basecoat and clearcoat, are then jointly cured to obtain a cured paint system.

SUMMARY
According to one embodiment of the present invention, a coating system is disclosed. The coating system includes a first layer, a second layer and a boundary layer. The first layer is comprised of a first coating composition including a first bulk polymer resin and a first reactive component selected from the group consisting of a part A reactive component and a part B reactive component.
The part A reactive component is reactive with the part B
reactive component. The second layer is of a second coating composition including a second bulk polymer resin and a second reactive component comprised of the unselected reactive component from the group consisting of the part A
reactive component and the part B reactive component. The boundary layer is formed upon applying the first layer of the first coating composition to the second layer of the second coating composition. The boundary layer includes the reaction product of the part A reactive component and the part B reactive component and is situated between the first layer and the second layer.

According to another embodiment of the present invention, a coating composition is disclosed for use in a wet on wet coating application process involving the application of a layer of the coating composition to an applied coating layer. The coating composition includes a bulk polymer resin and a reactive component selected from the group consisting of a part A reactive component and a part B.reactive component. The part A reactive component is reactive with the part B reactive component. The applied coating layer includes the other unselected reactive component from the group consisting of the part A reactive component and the part B reactive component. Upon applying a layer of the coating composition to the applied coating layer, a boundary layer is formed. The boundary layer includes the reaction product of the part A reactive component and the part B reactive component.
In one embodiment of the present invention, a wet on wet coating application method is disclosed. The method includes providing a first coating composition, a second coating composition and a substrate. The first coating composition includes a first bulk polymer resin and a first reactive component selected from the group consisting of a part A reactive component and a part B reactive component.
The part A reactive component is reactive with the part B
reactive component. The second coating composition includes a second bulk polymer resin and a second reactive component including the other, unselected reactive component from the group consisting of the part A reactive component and the part B reactive component. The method further includes applying the first coating composition to the substrate to form a first coating layer and applying the second coating composition to the first coating layer to form a second coating layer and to form a boundary layer situated between the first and second coating layers and comprising the reaction product of the reactive component and the unselected reactive component.
In another embodiment of the present invention, a coating system is disclosed. The coating system includes a
- 3 -first coating composition comprising a first bulk polymer resin, a part A reactive component and a part B reactive component. The part A reactive component is reactive with the part B reactive component. The coating system also includes a second coating composition comprising a second bulk polymer resin and a catalyst capable of catalyzing the reaction of the part A reactive component and the part B
reactive component. The coating system further includes a boundary layer formed upon interfacing a first layer of the first coating composition to a second layer of the second coating composition. The boundary layer includes the reaction product of the part A reactive component and the part B reactive component catalyzed by the catalyst and situated between the first layer and the second layer.
According to another embodiment of the present invention, a coating composition is disclosed for use in a wet on wet coating application process involving the application of a layer of the coating composition to a coating layer. The coating composition includes a bulk polymer resin, a part A reactive component, and a part B
reactive component. The part A reactive component is reactive with the part B reactive component. A coating layer comprising a catalyst is capable of catalyzing the reaction of the part A reactive component and the part B
reactive component. Upon interfacing a layer of the coating composition to the coating layer, a boundary layer is formed. The boundary layer includes the reaction product of the part A reactive component and the part B reactive component, catalyzed by the catalyst.
A wet on wet coating application method is disclosed according to one embodiment of the present invention. The method includes providing a first coating composition, a second coating composition and a substrate.
- 4 -The first coating composition includes a first bulk polymer resin, a part A reactive component, and a part B reactive component. The part A reactive component is reactive with the part B reactive component. The second coating composition includes a second bulk polymer resin and a catalyst capable of catalyzing the reaction of the part A
reactive component and the part B reactive component. The method further includes applying one of the first or second coating compositions to the substrate to form a first coating layer. The method also includes applying the other, unapplied composition of the first and second coating compositions to form a second coating layer and to form a boundary layer situated between the first and second coating layers and comprising the reaction product of the part A
reactive component and the part B reactive component, catalyzed by the catalyst.

DETAILED DESCRIPTION OF EMBODIMENTS OF THE PRESENT INVENTION
As required, detailed embodiments of the present invention are disclosed herein. However, it is to be understood that the disclosed embodiments are merely exemplary of the invention that may be embodied in various and alternative forms. Therefore, specific details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for the claims and/or as a representative basis for teaching one skilled in the art to variously employ aspects of the present invention.
Moreover, except for otherwise expressly indicated, all numeral quantities in this description indicating amounts of material are to be understood as modified the word "about"
in describing the broadest scope of the invention. Practice within the numerical limit stated is generally preferred.
- 5 -Unless expressly stated to the contrary: percent, "parts of," and ratio values are by weight; the term "polymer" includes "oligomer," "copolymer," "terpolymer,"
and the like; the description of a group or class of materials as suitable or preferred for a given purpose in connection with at least one aspect of the invention implies that mixtures of any two or more of the members of the group or class are equally suitable or preferred; description of constituents in chemical terms refers to the constituents at the time of addition to any combination specified in the description, and does not necessarily preclude chemical interactions among the constituents of a mixture once mixed;
and the first definition of an acronym or other abbreviation applies to all subsequent uses herein of the same abbreviation and applies mutatis mutandis to normal grammatical variations of the initially defined abbreviation.
Wet on wet systems may provide one or more benefits over a traditional system where a curing step typically occurs, e.g., between the application of the primer coat and basecoat. Heat-based curing methods, such as radiant, direct fire or infrared heating, are typically energy and capital intensive because of equipment requirements, the relatively large areas of factory floor space that are used, and the relatively high utility consumption. Energy and/or cost savings can be obtained by eliminating the curing step between the application of the wet coating layers. Moreover, one or more baking ovens, which are commonly used for curing the coating compositions, can be eliminated through the use of a wet on wet system.
In order to provide a cured paint system with an acceptable appearance and material performance, it is important to maintain the integrity of each wet layer
- 6 -without intrusion, commingling, and/or mixing (otherwise referred to as strike-in) of the previous layer with the subsequent layer. Strike-in between the wet coating layers may result in undesirable phenomena, such as reduced appearance quality and/or compromised properties of the cured coating layers. In extreme cases, such compromises in the coating layer properties may result in premature failure of the paint system.
According to current methods, layer separation may be achieved by air drying between application of layers and/or alternating chemical compositions of adjacent layers to achieve chemical separation of the layers. The air drying time, otherwise referred to as fiash time, may increase process cycle time and/or increase the process equipment and building footprint costs.
Accordingly, it is desirable, and there is a need, to provide a wet on wet paint application system and coating compositions for use in wet on wet paint application systems that minimize strike-in between wet coating layers such that the resulting paint system has acceptable properties.
Moreover, there is a need to provide a wet on wet paint application system and coating compositions for use in wet on wet paint application systems that do not require flash time between application of wet on wet layers.
One or more embodiments of the present invention address the problem of unacceptable processing times of wet on wet systems resulting from the necessity of flash times in order to minimize strike-in. While current methods sacrifice processing time to enable mitigation of strike-in, one or more embodiments of the present invention deliver reduced strike-in and processing time, thereby addressing a combination of problems not recognized or addressed by current methods. In one or more embodiments, the reduction
- 7 -or elimination of processing time, i.e., flash time, may reduce power consumption and costs compared to conventional paint methods and systems.
The present invention includes embodiments directed at wet on wet paint application systems and coating compositions for use in wet on wet paint application systems. The paint application systems and the coating compositions can be used as the external and/or internal finishes for consumer products, such as exterior surfaces of automotive vehicles.
In one embodiment of the present invention, a coating system for use in a wet on wet coating application process is disclosed. The coating system includes a first coating composition, a second coating composition and a boundary layer. The first coating composition includes a first bulk polymer resin and a first reactive component selected from a part A reactive component and a part B
reactive component group, which are reactive with each other. The second coating composition includes a second bulk polymer resin and a second reactive component being the other unselected member of the part A reactive component and the part B reactive component group. The boundary layer is formed upon applying a first layer of the first coating composition to a second layer of the second coating composition. The boundary layer includes the reaction product of the part A reactive component and the part B
reactive component and is situated between the first layer and the second layer. In one embodiment, the first coating composition is a basecoat and the second coating composition is a primer coat. In another embodiment, the first coating composition is a clearcoat and the second coating composition is a basecoat. The part A reactive component
- 8 -can be an isocyanate and the part B reactive component can be a polyol.
According to another embodiment of the present invention, a coating system for use in a wet on wet coating application process is disclosed. The coating system includes a first coating composition, a second coating composition and a boundary layer. The first coating composition includes a first bulk polymer resin, a part A
reactive component and a part B reactive component. The second coating composition includes a second bulk polymer resin and a catalyst capable of catalyzing the reaction between the part A reactive component and the part B
reactive component. The boundary layer is formed upon applying a first layer of the first coating composition to a second layer of a second coating composition. The boundary layer includes the reaction product of the part A reactive component and the part B reactive component catalyzed by the catalyst and is situated between the first layer and the second layer. In at least one embodiment, the first coating composition is a basecoat and the second coating composition is a primer coat. In another embodiment, the first coating composition is a clearcoat and the second coating composition is a basecoat.
In at least one embodiment, a wet on wet paint application system is disclosed that includes the application and curing of an electrocoat (ecoat) to a substrate (for example, the external surface of a vehicle panel), followed by the application of a wet primer coat to the cured ecoat, followed by the application of a basecoat to the at least substantially uncured primer coat, followed by the application of a clearcoat (otherwise referred to as a topcoat) to the at least substantially uncured basecoat, followed by the simultaneous curing of the at least
- 9 -substantially uncured primer coat, basecoat and clearcoat.
Non-limiting examples of other substrates that can be utilized in accordance with the present invention include sheet molding compound (SMC) substrates, GTX resin.
substrates, and other substrate materials that are suitable for the construction of automotive bodies.
The coating compositions of the present invention are typically applied at a sufficient thickness to produce a cured coating layer that is at least 0.5 mils thick and in some embodiments is less than 0.5 mils thick. When the curing composition is used as a primer coat, the thickness of the cured coating can be from 0.5 to 1.5 mils thick.
When the curing composition is used as a basecoat, the thickness of the cured coating can be from 0.4 to 1.6 mils thick. When the coating composition is used as a clearcoat, the thickness of the cured coating can be from 1.0 to 2.5 mils thick.
The coating compositions can contain a substantial amount of a polymer resin, otherwise referred to as a bulk polymer resin. When the coating composition is a basecoat, the bulk polymer resin can be a pigmented resin, for example, the resin can be an acrylic, a polyurethane, or a polyester. Other polymer resins that are known in the art as basecoat compositions include, but are not limited to, vinyls, polycarbonates, alkyds, and polysiloxanes. Basecoat polymers can be crosslinkable, and thus include one or more type of crosslinkable functional groups. Such groups include, for example, hydroxy, isocyanate, amine, epoxy, acid, anhydride, acrylate, vinyl, silane, and acetoacetate groups. These groups may be masked or blocked in such a way so that they are unblocked and available for the cross-linking reaction under the desired curing conditions, generally elevated temperatures. In certain embodiments,
- 10 -crosslinkable functional groups include hydroxy functional groups and amino functional groups. When the coating composition is a clearcoat, the bulk polymer resin can include carbonate functionality. The bulk polymer resin can be cured by any known mechanism or curing agent. In certain embodiments, the curing process occurs in bulk at an elevated temperature. The coating can be cured at a temperature of at least about 80 C, in certain embodiments at least about 100 C, and in other embodiments at least about 120 C. The curing time may vary depending on the particular components used and physical parameters such as the thickness of the layers. Typical curing times range from 15 to 60 minutes.
The components of the coating composition can be uniformly mixed, along with other ingredients. The components, in addition to a bulk polymer resin, can include, but are not limited to organic solvents, antioxidants, UV absorbers, light stabilizers, pigments, fillers, catalysts, rheology control agents, and adhesion promoters.
In at least one embodiment, the coating compositions (otherwise referred to as the first and second coating compositions) of adjacent wet coating layers (otherwise referred to as the first and second wet coating layers) include a part A-part B reactive component system.
The first coating composition can be a previous or subsequently applied layer in a sequential wet on wet application process, while the second coating composition can be the other of the applied layers. Upon application of the second coating layer, the part A-part B reactive component system reacts at the interface between the first and second wet coating layers to form a boundary layer to
- 11 -minimize migration and/or mixing, i.e., strike-in between the adjacent wet coating layers.
In at least one embodiment, the first coating composition contains a part A reactive component or the part B reactive component. In certain embodiments, the weight percent of the reactive component can be in the range of 10 to 70 weight percent. The first coating composition also contains a bulk polymer resin. In certain embodiments, the weight percent of the bulk polymer resin can be in the range of 30 to 90 weight percent.

The second coating composition contains the other reactive component. In certain embodiments, the weight percentage of the other reactive component can be in the range of 10 to 70 weight percent. The second coating composition also contains a bulk polymer resin. In certain embodiments, the weight percentage of the bulk polymer resin can be in the range of 30 to 90 weight percent.
According to one example, the first coating composition is a basecoat that contains a polyol as the part A reactive component at a 40 weight percent of the total weight of the first coating composition. In certain embodiments, the basecoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin. The second coating composition is a clearcoat that contains an isocyanate as the part B reactive component at a 30 weight percent of the total weight of the second coating composition. In certain embodiments, the clearcoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin.
In at least one embodiment, the first coating composition is a primer coat and the second coating composition is a basecoat.
- 12 -According to another example, the first coating composition is a primer coat and the second coating composition is a basecoat. Moreover, a third coating composition, i.e., a clearcoat is contemplated by the present invention, where each of the first, second and third coating compositions are sequentially applied as wet coating layers. Each of the coating compositions includes a reactive component. For example, the primer coat can contain a part A reactive component, the basecoat can contain a part B reactive component, and the clearcoat can contain a part A reactive component. After application of the three wet layers, a first and second boundary layer is formed between adjacent wet layers, i.e., primer coat/basecoat and basecoat/clearcoat.
It should be appreciated that any weight percentages of the part A and part B reactive components can be utilized provided that the weight percentages do not substantially affect the cure kinetics of the bulk polymer resins of the first and second coating compositions. The weight percentages are selected based on the reactivities of the part A and part B reactive components such that the reaction between the polyol and isocyanate occurs relatively quickly at room temperature to minimize strike-in between the adjacent wet layers, while not substantially affecting the curing of the bulk polymer resins, which occurs at an elevated temperature. For example, the reaction forming the boundary layer can occur in the range of 68 F to 75 F while the bulk curing can occur at a temperature of 80 F or higher. The time to form the boundary layer can be in the range of 1 to 10 minutes, and depends on the reactivity and cure kinetics of the part A-part B components, and the bulk polymer resins utilized. In certain embodiments, the
- 13 -thickness of the cured interface layer is in the range of 0.1 to 0.5 mils thick.
Other part A-part B reactive component systems are contemplated by the present invention. Non-limiting examples include isocyanate and thiol; epoxy and multifunctional acid; epoxy and thiol; epoxy and amine;
epoxy and anhydride; epoxy and polyol; blocked isocyanate and polyol; blocked isocyanate and thiol; acrylate and acetoacetate (Michaels addition reaction); and ketimine and acetoacetate.
Many of the reactive components identified above can be built into an acrylic backbone, such that the main polymer chain is an acrylic, with the reactive functional group being selected from a reactive component identified above. For instance, the main polymer chain in both reactive components of an epoxy and multifunctional acid system can be an acrylic with the functional groups being an epoxy on the A side (for example, an epoxy derived from a glycidyl methacrylate monomer) and a one or more carboxylic acid groups on the B side.
In at least one embodiment, the first and/or second coating compositions can further contain one or more catalysts for controlling the rate of reaction of the part A-part B reaction at the interface between the two adjacent wet layers. In at least one embodiment, the weight percentage of the catalyst is selected such that the reaction rate of the part A-part B reaction at the interface is controlled and/or increased while not substantially affecting the curing rate of the bulk polymer resins. In certain embodiments, the weight percentage of the interface catalyst can be in the range of 0.05 to 2 percent. It should be appreciated that each coating composition can also
- 14 -include a catalyst for controlling and/or increasing the curing reaction of the bulk polymer resin.
In at least one embodiment, a first coating composition can include a bulk polymer resin catalyst for catalyzing the bulk reaction and an interface catalyst for catalyzing the reaction at the interface between the layer and a subsequently applied wet layer. The weight percent of the bulk catalyst can be in the range of 0.05 to 2 weight percent. Non-limiting examples of interface catalysts include strong organic acids or tin-based compounds. Other examples include base catalysts, which can be used with the thiol/epoxy reaction.and the Michaels addition reaction, for example.

In at least one embodiment, the first coating composition contains the part A reactive component and the part B reactive component, each at a defined weight percentage relative to the total weight of the first coating composition. For example, the weight percentage of the part A reactive component can be in the range of 10 to 70 weight percentage and the weight percentage of the part B
reactive component can be in the range of 10 to 70 weight percentage. The first coating composition also contains a bulk polymer resin at a defined weight percentage relative to the total weight of the first coating composition. For example, the weight percentage of the bulk polymer resin can be in the range of 30 to 90 weight percent. The second coating composition contains a catalyst for catalyzing the reaction between the part A and part B reactive components.
The interface catalyst can be selected based on its ability to catalyze the part A-part B reaction so that it proceeds rapidly at the interface between the two layers while not increasing the rate of curing of the bulk polymer resins of the first and second coating compositions. The second
- 15 -coating composition contains a bulk polymer resin at a defined weight percentage relative to the total weight of the second coating composition. For example, the weight percent can be in the range of 30 to 90 weight percent.
The first coating composition can be applied as a previous or subsequently applied layer in a sequential wet on wet application process, while the second coating composition can be the other of the applied layers.
The first and second coating compositions can also include a first and second catalyst, respectively, for controlling and/or increasing the cure rate of the first and second bulk polymer resins, in addition to the interface catalyst for controlling and/or increasing the reaction rate of the part A-part B reaction.
According to one example, the first coating composition is a basecoat that contains a polyol as the part A reactive component at a 10 weight percent and an isocyanate as the part B reactive component at a 10 weight percent. In certain embodiments, the basecoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin. The second coating composition is a clearcoat that contains a tin-based catalyst at a 0.5 weight percent of the total weight of the second coating composition. In certain embodiments, the clearcoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin. The part A-part B reaction proceeds relatively quickly at the interface to form the boundary layer. In certain embodiments, the reaction time to form the boundary layer is in the range of 1 to 10 minutes.
Moreover, the tin-based catalyst does not substantially affect the rate of curing of the bulk polymer resins in the basecoat and clearcoat. Such curing occurs when the
- 16 -adjacent wet layers are subjected to elevated temperatures, for example, curing in a paint oven.
According to another example, the first coating composition is a basecoat that contains a part A-part B
reactive system that is base catalyzed, for example, an isocyanate/thiol system or a Michaels addition reaction system. In certain embodiments, the basecoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin. The second coating composition is a clearcoat that contains a base catalyst, for example, a tertiary amine, at a 0.5 weight percent of the total weight of the second coating composition. In certain embodiments, the clearcoat contains an isocyanate/polyol based polymer resin. Because of the presence of the base catalyst in the clearcoat, the part A-part B reaction proceeds relatively quickly at the interface to form the boundary layer at room temperature. In certain embodiments, the time to form the boundary layer is in the range of 1 to 10 minutes.
Moreover, the base catalyst does not substantially affect the rate of curing of the bulk polymer resins in the basecoat and clearcoat. Such curing occurs when the adjacent wet layers are subjected to a curing process at an elevated temperature.=
According to yet another example, the first coating composition is a basecoat that contains a part A-part B component reactive system that is base catalyzed, for example, a thiol/epoxy system, isocyanate/thiol system or a Michaels addition reaction system, and a photolatent base compound, for example, Irgacure 907 from Ciba Specialty Chemicals. In certain embodiments, the basecoat contains an acrylic compound with hydroxyl functionality mixed with a melamine resin. The second coating composition is a clearcoat. In certain embodiments, the clearcoat contains
- 17 -an isocyanate/polyol based polymer resin. After application of the adjacent wet coating layers, a UV light source can be directed at the wet coating layers, thereby at least partially liberating the photolatent base compound in a top portion of the basecoat to quickly cure the top portion, while opacity inhibits the cure in the rest of the basecoat.
The thickness of the top portion can be in the range of 1 to 20 percent of the total depth of the basecoat. Moreover, the opacity inhibits the cure in the rest of the basecoat and therefore, the UV light source does not substantially affect the rate of curing of the polymer resins in the basecoat and clearcoat. Such curing occurs when the adjacent wet layers are subjected to a curing process, for example, curing in a paint oven.
While embodiments of the invention have been illustrated and described, it is not intended that these embodiments illustrate and describe all possible forms of the invention. Rather, the words used in the specification are words of description rather than limitation, and it is understood that various changes may be made without departing from the spirit and scope of the invention.
- 18 -

Claims (23)

1. A coating system comprising:
a first layer of a first coating composition comprising:
a first bulk polymer resin; and a first reactive component selected from the group consisting of a part A reactive component and a part B
reactive component, wherein the part A reactive component is reactive with the part B reactive component, a second layer of a second coating composition comprising:
a second bulk polymer resin; and a second reactive component comprised of the unselected reactive component from the group consisting of the part A reactive component and the part B reactive component; and a boundary layer formed upon applying the first layer of the first coating composition to the second layer of the second coating composition, the boundary layer comprising the reaction product of the part A reactive component and the part B reactive component and being situated between the first layer and the second layer.
2. The coating system of claim 1, wherein the first coating composition is a basecoat and the second coating composition is a primer coat.
3. The coating system of claim 1, wherein the first coating composition is a clearcoat and the second coating composition is a basecoat.
4. The coating system of claim 1, wherein the part A reactive component is an isocyanate and the part B
reactive component is a polyol.
5. A coating composition for use in a wet on wet coating application process involving the application of a layer of the coating composition to an applied coating layer, the coating composition comprising:
a bulk polymer resin; and a reactive component selected from the group consisting of a part A reactive component and a part B
reactive component, wherein the part A reactive component being reactive with the part B reactive component, wherein an applied coating layer including the other unselected reactive component from the group consisting of the part A
reactive component and the part B reactive component, wherein upon applying a layer of the coating composition to the applied coating layer, forming a boundary layer comprising the reaction product of the part A reactive component and the part B reactive component.
6. The coating composition of claim 5, wherein the layer of the coating composition is a basecoat and the applied coating layer is a primer coat.
7. The coating composition of claim 5, wherein the layer of the coating composition is a clearcoat and the applied coating layer is a basecoat.
8. The coating composition of claim 5, wherein the part A reactive component is an isocyanate and the part B reactive component is a polyol.
9. A wet on wet coating application method comprising:
providing a first coating composition, a second coating composition and a substrate, wherein the first coating composition comprising: a first bulk polymer resin and a first reactive component selected from the group consisting of a part A reactive component and a part B
reactive component, wherein the part A reactive component being reactive with the part B reactive component, wherein the second coating composition comprising: a second bulk polymer resin and a second reactive component comprising the other, unselected reactive component from the group consisting of the part A reactive component and the part B
reactive component;
applying the first coating composition to the substrate to form a first coating layer; and applying the second coating composition to the first coating layer to form a second coating layer and to form a boundary layer situated between the first and second coating layers and comprising the reaction product of the reactive component and the unselected reactive component.
10. The method of claim 9, wherein the substrate is an ecoated substrate, the first layer is a primer coat and the second layer is a basecoat.
11. The method of claim 9, wherein the first layer is a basecoat and the second layer is a clearcoat.
12. The method of claim 9, further comprising forming the boundary layer situated between the first and second coating layers after applying the second coating composition to the first coating layer.
13. A coating system comprising:
a first coating composition comprising:
a first bulk polymer resin;
a part A reactive component; and a part B reactive component, wherein the part A reactive component is reactive with the part B reactive component;
a second coating composition comprising:
a second bulk polymer resin; and a catalyst capable of catalyzing the reaction of the part A reactive component and the part B reactive component; and a boundary layer formed upon interfacing a first layer of the first coating composition to a second layer of the second coating composition, the boundary layer comprising the reaction product of the part A reactive component and the part B reactive component catalyzed by the catalyst and situated between the first layer and the second layer.
14. The coating system of claim 13, wherein the first coating composition is a basecoat and the second coating composition is a primer coat.
15. The coating system of claim 13, wherein the first coating composition is a clearcoat and the second coating composition is a basecoat.
16. The coating system of claim 13, wherein the weight percent of the catalyst in the second coating composition is 0.05 to 2 weight percent.
17. A coating composition for use in a wet on wet coating application process involving the application of a layer of the coating composition to a coating layer, the coating composition comprising:
a bulk polymer resin;
a part A reactive component; and a part B reactive component, wherein the part A
reactive component is reactive with the part B reactive component, wherein the coating layer comprising a catalyst capable of catalyzing the reaction of the part A reactive component and the part B reactive component, wherein upon interfacing a layer of the coating composition to the coating layer, forming a boundary layer comprising the reaction product of the part A reactive component and the part B reactive component catalyzed by the catalyst.
18. The coating composition of claim 17, wherein the layer of the coating composition is a basecoat and the coating layer is a primer coat.
19. The coating composition of claim 17, wherein the layer of the coating composition is a clearcoat and the coating layer is a basecoat.
20. The coating composition of claim 17, wherein the part A reactive component is an isocyanate and the part B reactive component is a polyol.
21. A wet on wet coating application method comprising:
providing a first coating composition, a second coating composition and a substrate, wherein the first coating composition comprising: a first bulk polymer resin, a part A reactive component, and a part B reactive component, wherein the part A reactive component is reactive with the part B reactive component, wherein the second coating composition comprising a second bulk polymer resin and a catalyst capable of catalyzing the reaction of the part A reactive component and the part B reactive component;
applying one of the first or second coating compositions to the substrate to form a first coating layer;
and applying the other, unapplied composition of the first and second coating compositions to form a second coating layer and to form a boundary layer situated between the first and second coating layers and comprising the reaction product of the part A reactive component and the part B reactive component, catalyzed by the catalyst.
22. The method of claim 21, wherein the part A
reactive component is an isocyanate and the part B reactive component is a polyol.
23. The method of claim 21, further comprising forming the boundary layer situated between the first and second coating layers after the other, unapplied composition of the first or second coating compositions is applied.
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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090298962A1 (en) * 2006-09-29 2009-12-03 Katia Studer Photolatent bases for systems based on blocked isocyanates
CN103073975B (en) * 2012-10-15 2016-03-02 怀远县巨龙机械制造有限公司 A kind of Alkyd resin vehicle primer and preparation method thereof
KR102328478B1 (en) 2014-03-26 2021-11-18 쓰리엠 이노베이티브 프로퍼티즈 컴파니 Polyurethane compositions, films, and methods thereof
WO2019138876A1 (en) * 2018-01-11 2019-07-18 旭化成株式会社 Coating method and coating film
EP3757258A4 (en) * 2018-02-23 2022-01-19 Kansai Paint Co., Ltd Coating method for cationic electrodeposition coating material

Family Cites Families (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU575040B2 (en) 1983-03-10 1988-07-21 Basf Corporation Epsilon-caprolactone modified acrylic polymers
GB2171030B (en) * 1985-01-10 1988-09-28 Kansai Paint Co Ltd Coating method
US5147453A (en) 1987-11-03 1992-09-15 Basf Corporation Paint compositions containing silver metal flake pigment
BR9307855A (en) * 1993-05-21 1996-01-09 Kasai Paint Company Coating forming process
US5578345A (en) * 1993-11-24 1996-11-26 The Sherwin-Williams Company Multi-layer coating composition incorporating migratory catalyst
KR100186899B1 (en) 1994-10-28 1999-04-01 우노 마사야스 Curable base-coat composition method of film-forming and coated articles
US5962574A (en) 1997-07-25 1999-10-05 Bee Chemical Company Wet-on-wet primer with low film build U.V. light protection
US6184273B1 (en) 1997-09-30 2001-02-06 Basf Corporation Coating composition containing a compound with latent functionality
US5994469A (en) 1997-09-30 1999-11-30 Basf Corporation Curable coating composition containing a resin with latent functionality
DE19908001A1 (en) 1999-02-25 2000-08-31 Basf Coatings Ag Highly scratch-resistant multi-layer coating, process for their production and their use
DE19909894A1 (en) 1999-03-06 2000-09-07 Basf Coatings Ag Sol-gel coating for single-layer or multi-layer coatings
AU771282B2 (en) 1999-07-30 2004-03-18 Ppg Industries Ohio, Inc. Coating compositions having improved scratch resistance, coated substrates and methods related thereto
JP2003506518A (en) 1999-07-30 2003-02-18 ピーピージー インダストリーズ オハイオ, インコーポレイテッド Coating compositions with improved scratch resistance, coated substrates and related methods
DE60022765T2 (en) 1999-07-30 2006-06-29 Ppg Industries Ohio, Inc. Coating compositions with improved scratch resistance and coated surfaces
US6623791B2 (en) 1999-07-30 2003-09-23 Ppg Industries Ohio, Inc. Coating compositions having improved adhesion, coated substrates and methods related thereto
DE19940855A1 (en) 1999-08-27 2001-03-01 Basf Coatings Ag Solventborne coating material and its use
US6210758B1 (en) 1999-11-17 2001-04-03 Basf Corporation Composite coating with improved chip resistance
US6472493B1 (en) * 1999-11-23 2002-10-29 E. I. Du Pont De Nemours And Company Clear coating composition having improved early hardness and water resistance
EP1227113A4 (en) 1999-11-30 2003-03-19 Daicel Chem Lowly lactone-modified reactive monomer composition, acrylic polyol resins produced with the same, curable resin compositions and coating compositions
US6342144B1 (en) 1999-12-15 2002-01-29 Basf Aktiengesellschaft Cured multilayer coating and processing for its production
US6635341B1 (en) 2000-07-31 2003-10-21 Ppg Industries Ohio, Inc. Coating compositions comprising silyl blocked components, coating, coated substrates and methods related thereto
KR100545438B1 (en) 2000-09-22 2006-01-24 피피지 인더스트리즈 오하이오 인코포레이티드 Curable polyurethanes, coatings prepared therefrom, and method of making the same
WO2002024778A2 (en) 2000-09-22 2002-03-28 Ppg Industries Ohio, Inc. Curable polyurethanes, coatings prepared therefrom, and method of making the same
US6657007B2 (en) * 2000-09-29 2003-12-02 Basf Corporation Clearcoat composition with improved adhesion
US6541594B2 (en) 2000-12-19 2003-04-01 Basf Corporation Coating compositions containing crosslinkable monomeric difunctional compounds having at least thirty carbon atoms
US6740359B2 (en) 2001-02-06 2004-05-25 E. I. Du Pont De Nemours And Company Ambient cure fast dry solvent borne coating compositions
US6890586B2 (en) * 2001-08-21 2005-05-10 G.I. Plastek Limited Partnership System and method of making an in-mold clear-coated composite
US6555231B2 (en) 2001-07-03 2003-04-29 Basf Corporation Waterborne coating composition and a paint system thereof having improved chip resistance
US6592998B2 (en) 2001-07-31 2003-07-15 Ppg Industries Ohio, Inc. Multi-layer composites formed from compositions having improved adhesion, coating compositions, and methods related thereto
US6592999B1 (en) 2001-07-31 2003-07-15 Ppg Industries Ohio, Inc. Multi-layer composites formed from compositions having improved adhesion, coating compositions, and methods related thereto
JP3831266B2 (en) 2002-01-22 2006-10-11 日本ペイント株式会社 Coating method
US7342071B2 (en) 2002-10-31 2008-03-11 Basf Corporation Clearcoat paint composition
EP1569977B1 (en) * 2002-11-05 2008-06-11 The Sherwin-Williams Company Curable compositions
JP2004275965A (en) 2003-03-18 2004-10-07 Nippon Paint Co Ltd Method for forming coating film
US6894123B2 (en) 2003-03-21 2005-05-17 E.I. Du Pont De Nemours And Company Acetoacetylated polyvinyl polymers and curable coating compositions made therefrom
US20040228975A1 (en) 2003-05-13 2004-11-18 Shoichi Takesako Method for forming plural-layered coated film
DE602004002720T8 (en) 2003-05-19 2008-01-17 Kansai Paint Co., Ltd., Amagasaki A method of electrostatically coating a plastic article
US6989421B2 (en) 2003-07-02 2006-01-24 E. I. Dupont Denemours And Company Two component coating compositions and coatings produced therefrom
US6933005B2 (en) * 2003-09-22 2005-08-23 E. I. Du Pont De Nemours And Company Method for achieving recoat adhesion over a fluorinated topcoat
US7071286B2 (en) 2003-12-02 2006-07-04 E. I. Dupont De Nemours And Company Coating compositions with high solids content for vehicle coating
US7091278B2 (en) 2003-12-10 2006-08-15 E. I. Dupont De Nemours And Company Aqueous two-component coating compositions
US7157536B2 (en) 2004-01-19 2007-01-02 E. I. Du Pont De Nemours And Company Coating composition for ambient cure containing an alkoxylated amine
US20050159625A1 (en) 2004-01-19 2005-07-21 Coates John S. Alkoxylated amine and process therefor
EP1765951A1 (en) 2004-06-18 2007-03-28 Akzo Nobel Coatings International BV Multilayer coating system
US7071242B2 (en) 2004-10-13 2006-07-04 E. I. Dupont De Nemours And Company Process for the production of polyurethane di(meth)acrylates
US7166748B2 (en) 2004-12-15 2007-01-23 E.I. Dupont De Nemours & Co. Durable coating compositions containing novel aspartic amine compounds
US7214828B2 (en) 2004-12-15 2007-05-08 E. I. Dupont De Nemours And Company Durable coating compositions containing novel aspartic amine compounds

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ES2491240T3 (en) 2014-09-05
CN101117547A (en) 2008-02-06
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US20080032057A1 (en) 2008-02-07
US20150307740A1 (en) 2015-10-29

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