EP0525867A1 - Two-layer coating systems for wheels and architectural applications - Google Patents

Two-layer coating systems for wheels and architectural applications Download PDF

Info

Publication number
EP0525867A1
EP0525867A1 EP92202190A EP92202190A EP0525867A1 EP 0525867 A1 EP0525867 A1 EP 0525867A1 EP 92202190 A EP92202190 A EP 92202190A EP 92202190 A EP92202190 A EP 92202190A EP 0525867 A1 EP0525867 A1 EP 0525867A1
Authority
EP
European Patent Office
Prior art keywords
coating layer
layer
coating
resin
coating system
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP92202190A
Other languages
German (de)
French (fr)
Other versions
EP0525867B1 (en
Inventor
Dominique Durand
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Akzo Nobel NV
Original Assignee
Akzo NV
Akzo Nobel NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Akzo NV, Akzo Nobel NV filed Critical Akzo NV
Publication of EP0525867A1 publication Critical patent/EP0525867A1/en
Application granted granted Critical
Publication of EP0525867B1 publication Critical patent/EP0525867B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • B05D7/53Base coat plus clear coat type
    • B05D7/532Base coat plus clear coat type the two layers being cured or baked together, i.e. wet on wet
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D5/00Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
    • B05D5/06Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
    • B05D5/067Metallic effect
    • B05D5/068Metallic effect achieved by multilayers
    • 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
    • B05D7/53Base coat plus clear coat type
    • B05D7/536Base coat plus clear coat type each layer being cured, at least partially, separately
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2451/00Type of carrier, type of coating (Multilayers)
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D2601/00Inorganic fillers
    • B05D2601/02Inorganic fillers used for pigmentation effect, e.g. metallic effect
    • B05D2601/04Mica

Definitions

  • the present invention relates to a multilayer coating system which is suitable, e.g., for covering wheels for cars or for use in architectural applications, particularly involving aluminum substrates.
  • Such coating systems should possess a good combination of properties such as total layer thickness, metallic lustre, stone-chipping resistance, corrosion resistance, petrol resistance and outdoor durability.
  • Known systems are normally based upon at least three coating layers including a first coating layer which provides generally the basic color and opacifying of the substrate, a second liquid layer which provides a metallized effect and, finally, a third liquid clear varnish which provides certain appearance and protective aspects required for the particular end use.
  • the known systems do not always possess a desired combination of the aforementioned properties and, in addition, the application of so many coating layers can result in technical problems.
  • an object of the present invention to provide a two-layer coating system which surprisingly possesses a more desirable combination of the aforementioned properties.
  • the two-layer coating systems in according with the present invention consist essentially of:
  • This coating system results in a desirable combination of properties such as weatherability, corrosion resistance, stone-chipping resistance and appearance characteristics.
  • the first coating layer in accordance with the present invention provides the basic color of the two-layer coating system as well as opacifying of the substrate.
  • the first coating layer may comprise a cathodic electrodeposition coating layer or a powder coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin, such layers and resins being generally well-known in the art.
  • the second metallized transparent powder coating layer is preferably based upon any one of a number of polyester resins, epoxy resins, acrylate resins and/or polyurethane resins known for use in powder coatings for producing transparent layers, and optionally a curing agent for that resin.
  • polyester resins are particularly preferred.
  • the polyester resin can be a hydroxylated polyester in combination with a hydroxyl group reactive curing agent, but preferably is a carboxylated polyester in combination with a carboxyl group reactive curing agent.
  • a very suitable powder coating system for the second layer comprises a carboxylated polyester and an epoxy compound as curing agent.
  • Suitable polyesters can be obtained via customary preparation processes from by preference substantially aromatic polycarboxylic acids and a variety of polyols.
  • aromatic polycaboxylic acids may be mentioned phthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 3,6-dich- lorophthalic acid, terechlorophthalic acid and, in so far as available, the anhydrides, acid chlorides and lower alkyl esters thereof.
  • cycloaliphatic and/or acylic polycarboxylic acids may be utilized in amounts up to 30 mol%, and preferably up to 20 mol%, based upon the total moles of carboxylic acids utilized.
  • cycloaliphatic and/or acyclic polycarboxylic acids may be mentioned tetrahydrophthalic acid, hexahydroendomethylene tetrahydrophthalic acid, azeleic acid, sebacic acid, decanedicarboxylic acid, dimeric fatty acids, adipic acid, succinic acid and maleic acid.
  • Hydroxycarboxylic acids and/or lactones such as 12-hydroxystearic, E -caprolactone and the hydropivalic acid ester of neopentyl glycol, as well as monocarboxylic acids such as benzoic acid, tert.-butyl benzoic acid, hexahydrobenzoic acid and saturated aliphatic monocarboxylic acids, can also be utilized in minor amounts.
  • aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butane-1,3-diol, 2,2-dimethyl propane-1,3-diol (neopentyl glycol), hexane-2,5-diol, hexane-1,6-diol and diethylene glycol; and cycloaliphatic and aromatic diols such as 1,4-dimethylol cyclohexane, 2,2-bis(4-hydroxycyclohexyl) propane and 2,2-bis-[4-(2-hydroxyethoxy)phenyl] propane.
  • aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butan
  • polyol component comprises at least 50 mol% of neopentyl glycol and/or propylene glycol, mol% here being based upon the total moles of polyols utilized.
  • the polyesters may be prepared by esterification and/or transesterification, optionally in the presence of customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate, in which processes, owing to a suitable choice of the preparation conditions and of the COOH/OH ratio, end products are obtained the acid value of which is preferably between 5 and 150 (mg KOH/g resin), and which are preferably carboxyl group terminated.
  • customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate
  • the preferred curing agent for the carboxylated polyester is an epoxy compound such as triglycidylisocyanurate or a heterocyclic triepoxy compound, such as methyl- substituted triglycidylisocyanurate or 1,2,4- triglycidyltriazolidine-3,5-dion or diglycidyl-terephthalate or an epoxy resin based on bisphenol A and epichlorohydrin, of which triglycidylisocyanurate is preferred.
  • the amount of epoxy compound utilized depends on the acid value of the polyester resin and on the epoxy equivalent weight of the epoxy compound.
  • the epoxy compound is utilized in amounts ranging between 0,8 and 1,2 equivalent epoxy per equivalent carboxyl group.
  • the second metallized transparent powder coating layer contains a mica pigment which is responsible for the metallization.
  • Mica is a well known class of minerals. Most micas are predominantly aluminium silicates of potassium, iron, lithium or fluorine. Since the chemical compositions are quite variable, mica may range from colorless and transparent to highly coloured, opaque varieties. According to a preferred embodiment of the present invention, the mica comprises platelets of mica coated with titanium dioxide.
  • the amount of mica utilized in the second layer is between 0,5 and 10% by weight based upon the total weight of the second layer.
  • carboxylated polyesters are mixed via, for example, extrusion and at a temperature of from 110-1300 C, with a polyepoxide, eventually pigments and other additives.
  • the mica pigment which is responsible for the metallization can be added at different places in the powder coating preparation.
  • the addition can take place as an internal metallization before the extrusion, as an external metallization after grinding or a combination of the external and internal metallization.
  • the external metallization is used.
  • Suitable pigments are, for instance, inorganic pigments such as titanium dioxide, zinc sulphide, iron oxide and chromium oxide, and organic pigments such as azo compounds.
  • Suitable fillers are, for instance, quartz powder, calcium and magnesium silicates, calcium carbonate, barium sulphate, calcium sulphate and aluminium oxide and mixtures of these optionally with smaller amounts of, e.g., aluminium hydroxide, am- moniumpolyphosphate and the like.
  • Suitable flow-promoting agents are, for instance, liquid polyacrylates such as, for instance, polybutylacrylate and polyethylacrylate, fluorinated polymers such as, for instance, esters of polyethylene glycol and perfluoroctanoic acid and polymeric siloxanes such as, for instance, polydimethyl siloxane or polymethylphenyl siloxane.
  • the powder coatings utilized for the second coating layer are preferably applied to the first coating layer by electrostatic/tribo spraying and cured at temperatures between 160-200 °C under the influence of a catalyst. During the curing process, the powder coating melts and subsequently flows out to form a smooth, continuous coating film before substantial curing of the components.
  • Suitable catalysts must guarantee rapid curing of the components but must be substantially inactive in the mixing of the polyester and epoxy resins.
  • the first layer Prior to application of the second coating layer, the first layer can be a cured layer but also a non-or partially cured layer.
  • An advantage of the present two-layer coating system is the possibility to cure both layers in one step, in which case the first layer is applied as a base, over which the second metallized transparent powder coating is applied, after which the total system is cured under the aforementioned conditions.
  • the two-layer coating system according to the invention is applied onto an aluminum substrate; however, the system can also be applied on other substrates such as iron, steel, copper, carbon, wood, glass and polymers.
  • a cathodic electrodeposition layer as the first layer, especially one based upon an epoxy resin and optional curing agent therefor.
  • a cathodic electrodeposition layer based upon an aqueous dispersion or solution of an epoxy resin.
  • the thickness of the cathodic electrodeposition first layer is between 15 and 30 ⁇ m
  • the thickness of the second metallized transparent powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 /1.m)
  • the total thickness of the two-layer system is between 45 and 130 ⁇ m (and more preferably between 55 and 100 /1.m).
  • the two-layer coating system When the two-layer coating system is utilized in architectural applications, it has been found most advantageous to utilize as the first layer another powder coating based on an epoxy resin, polyester resin, polyacrylate resin and/or polyurethane resin, and optionally a curing agent therefor.
  • This first powder coating layer can contain the already mentioned customary additives, and especially a pigment to obtain a color.
  • the thickness of the first powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 ⁇ m), and the thickness of the second metallized transparent powder coating layer is between 30 and 100 ⁇ m (and more preferably between 40 and 70 ⁇ m).
  • a wheel was provided with a cathodic electrodeposition layer based on an epoxy resin.
  • a powder coating based on a polyester and TGIC weight ratio polyester: TGIC 93 : 7 and mica ('Mearlin superwhite') was applied in a weight ratio polyester/TGIC: Mica 95 : 5 by tribospraying in a layer thickness of 45 /1.m.
  • Curing conditions 10 minutes, 180°C, infrared curing.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Laminated Bodies (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

The present invention relates to a two-layer coating system consisting essentially of (a) a first coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin; and (b) a second metallized transparent powder coating layer containing a mica pigment. This two-layer coating system is particularly suited for aluminum substrates such as wheels for cars and in architectural applications.

Description

  • The present invention relates to a multilayer coating system which is suitable, e.g., for covering wheels for cars or for use in architectural applications, particularly involving aluminum substrates.
  • Such coating systems should possess a good combination of properties such as total layer thickness, metallic lustre, stone-chipping resistance, corrosion resistance, petrol resistance and outdoor durability.
  • Known systems are normally based upon at least three coating layers including a first coating layer which provides generally the basic color and opacifying of the substrate, a second liquid layer which provides a metallized effect and, finally, a third liquid clear varnish which provides certain appearance and protective aspects required for the particular end use. The known systems, however, do not always possess a desired combination of the aforementioned properties and, in addition, the application of so many coating layers can result in technical problems.
  • It is, therefore, an object of the present invention to provide a two-layer coating system which surprisingly possesses a more desirable combination of the aforementioned properties.
  • The two-layer coating systems in according with the present invention consist essentially of:
    • (a) a first coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin; and
    • (b) a second metallized transparent powder coating layer containing a mica pigment.
  • The use of this coating system results in a desirable combination of properties such as weatherability, corrosion resistance, stone-chipping resistance and appearance characteristics.
  • The first coating layer in accordance with the present invention provides the basic color of the two-layer coating system as well as opacifying of the substrate. Depending on the desired end use, the first coating layer may comprise a cathodic electrodeposition coating layer or a powder coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin, such layers and resins being generally well-known in the art.
  • The second metallized transparent powder coating layer is preferably based upon any one of a number of polyester resins, epoxy resins, acrylate resins and/or polyurethane resins known for use in powder coatings for producing transparent layers, and optionally a curing agent for that resin. Of these, the polyester resins are particularly preferred.
  • The polyester resin can be a hydroxylated polyester in combination with a hydroxyl group reactive curing agent, but preferably is a carboxylated polyester in combination with a carboxyl group reactive curing agent. A very suitable powder coating system for the second layer comprises a carboxylated polyester and an epoxy compound as curing agent.
  • Suitable polyesters can be obtained via customary preparation processes from by preference substantially aromatic polycarboxylic acids and a variety of polyols.
  • As aromatic polycaboxylic acids may be mentioned phthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 3,6-dich- lorophthalic acid, terechlorophthalic acid and, in so far as available, the anhydrides, acid chlorides and lower alkyl esters thereof.
  • In addition to the aromatic acids, cycloaliphatic and/or acylic polycarboxylic acids may be utilized in amounts up to 30 mol%, and preferably up to 20 mol%, based upon the total moles of carboxylic acids utilized. As examples of cycloaliphatic and/or acyclic polycarboxylic acids may be mentioned tetrahydrophthalic acid, hexahydroendomethylene tetrahydrophthalic acid, azeleic acid, sebacic acid, decanedicarboxylic acid, dimeric fatty acids, adipic acid, succinic acid and maleic acid. Hydroxycarboxylic acids and/or lactones such as 12-hydroxystearic, E-caprolactone and the hydropivalic acid ester of neopentyl glycol, as well as monocarboxylic acids such as benzoic acid, tert.-butyl benzoic acid, hexahydrobenzoic acid and saturated aliphatic monocarboxylic acids, can also be utilized in minor amounts.
  • As suitable polyols may be mentioned aliphatic diols such as ethylene glycol, propane-1,2-diol, propane-1,3-diol, butane-1,2-diol, butane-1,4-diol, butane-1,3-diol, 2,2-dimethyl propane-1,3-diol (neopentyl glycol), hexane-2,5-diol, hexane-1,6-diol and diethylene glycol; and cycloaliphatic and aromatic diols such as 1,4-dimethylol cyclohexane, 2,2-bis(4-hydroxycyclohexyl) propane and 2,2-bis-[4-(2-hydroxyethoxy)phenyl] propane. In addition, smaller amounts of higher functional polyols may also be utilized such as glycerol, hexanetriol, pentaerythritol, sorbitol, trimethylol ethane, trimethylol propane and tris-(2-hydroxy)isocyanurate. Epoxy compounds may also be utilized as polyols. Preferably, the polyol component comprises at least 50 mol% of neopentyl glycol and/or propylene glycol, mol% here being based upon the total moles of polyols utilized.
  • Using processes known per se the polyesters may be prepared by esterification and/or transesterification, optionally in the presence of customary catalyst such as, for instance, dibutyl tin oxide or tetrabutyltitanate, in which processes, owing to a suitable choice of the preparation conditions and of the COOH/OH ratio, end products are obtained the acid value of which is preferably between 5 and 150 (mg KOH/g resin), and which are preferably carboxyl group terminated.
  • As indicated above, the preferred curing agent for the carboxylated polyester is an epoxy compound such as triglycidylisocyanurate or a heterocyclic triepoxy compound, such as methyl- substituted triglycidylisocyanurate or 1,2,4- triglycidyltriazolidine-3,5-dion or diglycidyl-terephthalate or an epoxy resin based on bisphenol A and epichlorohydrin, of which triglycidylisocyanurate is preferred. The amount of epoxy compound utilized depends on the acid value of the polyester resin and on the epoxy equivalent weight of the epoxy compound. Preferably, the epoxy compound is utilized in amounts ranging between 0,8 and 1,2 equivalent epoxy per equivalent carboxyl group.
  • As also indicated above, the second metallized transparent powder coating layer contains a mica pigment which is responsible for the metallization. Mica is a well known class of minerals. Most micas are predominantly aluminium silicates of potassium, iron, lithium or fluorine. Since the chemical compositions are quite variable, mica may range from colorless and transparent to highly coloured, opaque varieties. According to a preferred embodiment of the present invention, the mica comprises platelets of mica coated with titanium dioxide.
  • Preferably the amount of mica utilized in the second layer is between 0,5 and 10% by weight based upon the total weight of the second layer.
  • The preparation of powder coatings based upon carboxylated polyesters and epoxy resins is generally well-known in the art. Preferably, the carboxylated polyesters are mixed via, for example, extrusion and at a temperature of from 110-1300 C, with a polyepoxide, eventually pigments and other additives.
  • The mica pigment which is responsible for the metallization can be added at different places in the powder coating preparation. The addition can take place as an internal metallization before the extrusion, as an external metallization after grinding or a combination of the external and internal metallization. Peferably the external metallization is used.
  • Other normal additives such as, for instance, other pigments, fillers, anti-oxidants, colorants, flow-promoting agents, release agents, viscosity agents, levelling agents and UV-stabilizers can be added to the coating systems of the two-layers.
  • Suitable pigments are, for instance, inorganic pigments such as titanium dioxide, zinc sulphide, iron oxide and chromium oxide, and organic pigments such as azo compounds.
  • Suitable fillers are, for instance, quartz powder, calcium and magnesium silicates, calcium carbonate, barium sulphate, calcium sulphate and aluminium oxide and mixtures of these optionally with smaller amounts of, e.g., aluminium hydroxide, am- moniumpolyphosphate and the like.
  • Suitable flow-promoting agents are, for instance, liquid polyacrylates such as, for instance, polybutylacrylate and polyethylacrylate, fluorinated polymers such as, for instance, esters of polyethylene glycol and perfluoroctanoic acid and polymeric siloxanes such as, for instance, polydimethyl siloxane or polymethylphenyl siloxane.
  • Of course, with respect to the second coating layer these additives should not substantially affect the transparent nature thereof.
  • The powder coatings utilized for the second coating layer are preferably applied to the first coating layer by electrostatic/tribo spraying and cured at temperatures between 160-200 °C under the influence of a catalyst. During the curing process, the powder coating melts and subsequently flows out to form a smooth, continuous coating film before substantial curing of the components.
  • Suitable catalysts must guarantee rapid curing of the components but must be substantially inactive in the mixing of the polyester and epoxy resins.
  • Prior to application of the second coating layer, the first layer can be a cured layer but also a non-or partially cured layer. An advantage of the present two-layer coating system, however, is the possibility to cure both layers in one step, in which case the first layer is applied as a base, over which the second metallized transparent powder coating is applied, after which the total system is cured under the aforementioned conditions.
  • Preferably the two-layer coating system according to the invention is applied onto an aluminum substrate; however, the system can also be applied on other substrates such as iron, steel, copper, carbon, wood, glass and polymers.
  • When the two-layer coating system is applied onto wheels for cars, it has been found most advantageous to utilize a cathodic electrodeposition layer as the first layer, especially one based upon an epoxy resin and optional curing agent therefor. Particularly preferred is a cathodic electrodeposition layer based upon an aqueous dispersion or solution of an epoxy resin.
  • Preferably, the thickness of the cathodic electrodeposition first layer is between 15 and 30 µm, the thickness of the second metallized transparent powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 /1.m), and the total thickness of the two-layer system is between 45 and 130 µm (and more preferably between 55 and 100 /1.m).
  • When the two-layer coating system is utilized in architectural applications, it has been found most advantageous to utilize as the first layer another powder coating based on an epoxy resin, polyester resin, polyacrylate resin and/or polyurethane resin, and optionally a curing agent therefor.
  • This first powder coating layer can contain the already mentioned customary additives, and especially a pigment to obtain a color.
  • Preferably, the thickness of the first powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 µm), and the thickness of the second metallized transparent powder coating layer is between 30 and 100 µm (and more preferably between 40 and 70 µm).
  • This system results in an excellent aspect of the powder layer for architectural uses. Furthermore the adhesion between the two layers is very good.
  • The invention will be further elucidated by means of the following examples, without, however, being limited thereto.
  • Example
  • A wheel was provided with a cathodic electrodeposition layer based on an epoxy resin. Next, a powder coating based on a polyester and TGIC (weight ratio polyester: TGIC 93 : 7) and mica ('Mearlin superwhite') was applied in a weight ratio polyester/TGIC: Mica 95 : 5 by tribospraying in a layer thickness of 45 /1.m.
  • Curing conditions: 10 minutes, 180°C, infrared curing.
  • The coating system resulted in the following characteristics:
    • - weatherability (according to the Peugeot method; xenon with 500 hours exposure) : loss of gloss 2%
    • - salt spray resistance (ASTM B 117) 800 hours: disbonding less than 0,5 mm, no blistering
    • - stone-chipping resistance (Peugeot method) : 1 (1 = excellent, 2 = very good, whereas 10 = very bad).

Claims (14)

1. A multilayer coating system comprising at least (a) a first layer and (b) a second metallized coating layer, characterized in that the coating system is a two-layer coating system consisting essentially of:
(a) a first coating layer based on an epoxy resin, alkyd resin, polyester resin, melamine-containing resin, polyurethane resin and/or polyacrylate resin; and
(b) a second metallized transparent powder coating layer containing a mica pigment.
2. The coating system according to claim 1, characterized in that the mica pigment comprises platelts of mica coated with titanium dioxide.
3. The coating system according to any one of claims 1-2, characterized in that the first coating layer is based on an epoxy resin.
4. The coating system according to any one of claims 1-3, characterized in that the second metallized transparent powder coating layer is based upon a polyester resin and a curing agent therefor.
5. The coating system according to claim 5, characterized in that the polyester resin is a carboxylated polyester resin and the curing agent is an epoxy resin.
6. The coating system according to any one of claims 1-5, characterized in that the first coating layer is a cathodic electrodeposition layer.
7. The coating system according to claim 6, characterized in that the first coating layer comprises a thickness between 15 and 30 µm, the second metallized transparent powder coating layer comprises a thickness between 30 and 100 µm, and the two-layer coating system comprises a total thickness between 45 and 130 tim.
8. The coating system according to any one of claims 1-5, characterized in that the first coating layer is powder coating layer.
9. The coating system according to claim 8, characterized in that the first coating layer comprises a thickness between 30 and 100 µm, and the second metallized transparent powder coating layer comprises a thickness between 30 and 100 µm.
10. A substrate coated with the two-layer coating system according to any one of claims 1-9.
11. The coated susbtrate according to claim 10, characterized in that the substrate is aluminum.
12. A wheel comprising the coated substrate according to any one of claims 10-11.
13. A method of producing the coated substrate according to any one of claims 10-12, characterized in that the first coating layer is applied onto the substrate, the second metallized transparent powder coating layer is applied onto the first coating layer which has optionally been partially or fully cured, then curing the system.
14. The method according to claim 13, characterized in that the second metallized transparent powder coating layer is applied onto a first coating layer which has not been cured.
EP19920202190 1991-07-26 1992-07-17 Two-layer coating systems for wheels and architectural applications Expired - Lifetime EP0525867B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP91201959 1991-07-26
EP91201959 1991-07-26

Publications (2)

Publication Number Publication Date
EP0525867A1 true EP0525867A1 (en) 1993-02-03
EP0525867B1 EP0525867B1 (en) 1995-12-06

Family

ID=8207802

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19920202190 Expired - Lifetime EP0525867B1 (en) 1991-07-26 1992-07-17 Two-layer coating systems for wheels and architectural applications

Country Status (4)

Country Link
EP (1) EP0525867B1 (en)
CA (1) CA2074661A1 (en)
DE (1) DE69206509T2 (en)
ES (1) ES2080432T3 (en)

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0646420A1 (en) * 1993-09-17 1995-04-05 Herberts Gesellschaft mit beschränkter Haftung Process for making multilayer coatings
FR2715160A1 (en) * 1994-01-19 1995-07-21 Montupet Sa Wheel or body element or metal accessory, for a motor vehicle, coated with an iridescent metallic paint and method of manufacture.
WO1997030796A1 (en) * 1996-02-23 1997-08-28 Basf Coatings Ag Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material
GB2328628A (en) * 1997-08-27 1999-03-03 Nippon Paint Co Ltd Powder coating method
GB2342600A (en) * 1998-10-08 2000-04-19 Thorstone Business Man Ltd Coatings
US6068890A (en) * 1996-07-31 2000-05-30 Dr. Ing. H.C.F. Porsche Ag Method for gloss coating articles
GB2369790A (en) * 2000-12-08 2002-06-12 Northpoint Ltd Method of protecting a surface
US6413588B1 (en) 1999-01-11 2002-07-02 E. I. Du Pont De Nemours And Company Method of producing durable layered coatings
GB2379897A (en) * 2001-08-31 2003-03-26 Kansai Paint Co Ltd Multilayer decorative coating including electrodeposited layer
US6641666B2 (en) 1999-11-15 2003-11-04 Ppg Industries Ohio, Inc. Method and apparatus for coating a substrate
WO2005120724A1 (en) * 2004-06-05 2005-12-22 Basf Coatings Ag Method for coating electrically conductive substrates
US7445816B2 (en) 1999-11-15 2008-11-04 Ppg Industries Ohio, Inc. Method and apparatus for coating a substrate
EP2153911A1 (en) * 2008-08-05 2010-02-17 Pulverit S.p.A. Painting/coating process using a powder primer with high reactivity, polymerisable in a single step with the finishing coat
WO2018226421A1 (en) * 2017-06-07 2018-12-13 Novelis Inc. Multi-layered finishes for can ends
IT202000005629A1 (en) * 2020-03-17 2021-09-17 La Bottega S R L "METHOD OF PRODUCTION OF AN OBJECT COVERED WITH A PAINTED LAYER"

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1769867A1 (en) * 1968-07-27 1971-02-11 Metallgesellschaft Ag Process for the production of colored plastic coatings
DE3324726A1 (en) * 1983-07-08 1985-01-17 Bosch-Siemens Hausgeräte GmbH, 7000 Stuttgart Process for the production of a multi-layer coating on a substrate to be coated by powder coating in an electrostatic field
EP0186607A1 (en) * 1984-12-11 1986-07-02 Basf Corporation Multilayer satin finish automotive paint system
DE3814853A1 (en) * 1987-05-02 1988-11-10 Kansai Paint Co Ltd COATING PROCESS

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1769867A1 (en) * 1968-07-27 1971-02-11 Metallgesellschaft Ag Process for the production of colored plastic coatings
DE3324726A1 (en) * 1983-07-08 1985-01-17 Bosch-Siemens Hausgeräte GmbH, 7000 Stuttgart Process for the production of a multi-layer coating on a substrate to be coated by powder coating in an electrostatic field
EP0186607A1 (en) * 1984-12-11 1986-07-02 Basf Corporation Multilayer satin finish automotive paint system
DE3814853A1 (en) * 1987-05-02 1988-11-10 Kansai Paint Co Ltd COATING PROCESS

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0646420A1 (en) * 1993-09-17 1995-04-05 Herberts Gesellschaft mit beschränkter Haftung Process for making multilayer coatings
FR2715160A1 (en) * 1994-01-19 1995-07-21 Montupet Sa Wheel or body element or metal accessory, for a motor vehicle, coated with an iridescent metallic paint and method of manufacture.
EP0664163A1 (en) * 1994-01-19 1995-07-26 Montupet S.A. Wheel, vehicle body element or metallic part, for vehicles, coated with metallic iridescent paint and process for manufacturing it
WO1997030796A1 (en) * 1996-02-23 1997-08-28 Basf Coatings Ag Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material
US6254751B1 (en) 1996-02-23 2001-07-03 Basf Coatings Ag Process for the multi-layered coating of substrates with electrophoretic coating material and powder coating material
US6068890A (en) * 1996-07-31 2000-05-30 Dr. Ing. H.C.F. Porsche Ag Method for gloss coating articles
US6238786B1 (en) 1996-07-31 2001-05-29 Dr. Ing. H.C.F. Porsche Ag Method for gloss coating articles
GB2328628A (en) * 1997-08-27 1999-03-03 Nippon Paint Co Ltd Powder coating method
US6025035A (en) * 1997-08-27 2000-02-15 Nippon Paint Co., Ltd. Electrostatic coating method and coating film
GB2328628B (en) * 1997-08-27 2001-10-10 Nippon Paint Co Ltd Paint film-forming method and paint film
GB2342600A (en) * 1998-10-08 2000-04-19 Thorstone Business Man Ltd Coatings
GB2342600B (en) * 1998-10-08 2003-03-19 Thorstone Business Man Ltd Coatings
US6413588B1 (en) 1999-01-11 2002-07-02 E. I. Du Pont De Nemours And Company Method of producing durable layered coatings
US6641666B2 (en) 1999-11-15 2003-11-04 Ppg Industries Ohio, Inc. Method and apparatus for coating a substrate
US7445816B2 (en) 1999-11-15 2008-11-04 Ppg Industries Ohio, Inc. Method and apparatus for coating a substrate
GB2369790A (en) * 2000-12-08 2002-06-12 Northpoint Ltd Method of protecting a surface
GB2379897A (en) * 2001-08-31 2003-03-26 Kansai Paint Co Ltd Multilayer decorative coating including electrodeposited layer
GB2379897B (en) * 2001-08-31 2005-07-13 Kansai Paint Co Ltd Method for forming multilayer coating film
WO2005120724A1 (en) * 2004-06-05 2005-12-22 Basf Coatings Ag Method for coating electrically conductive substrates
US7862851B2 (en) 2004-06-05 2011-01-04 Basf Coatings Ag Process for coating electrically conductive substrates
EP2153911A1 (en) * 2008-08-05 2010-02-17 Pulverit S.p.A. Painting/coating process using a powder primer with high reactivity, polymerisable in a single step with the finishing coat
WO2018226421A1 (en) * 2017-06-07 2018-12-13 Novelis Inc. Multi-layered finishes for can ends
US11065843B2 (en) 2017-06-07 2021-07-20 Novelis Inc. Multi-layered finishes for can ends
IT202000005629A1 (en) * 2020-03-17 2021-09-17 La Bottega S R L "METHOD OF PRODUCTION OF AN OBJECT COVERED WITH A PAINTED LAYER"

Also Published As

Publication number Publication date
EP0525867B1 (en) 1995-12-06
DE69206509D1 (en) 1996-01-18
DE69206509T2 (en) 1996-08-01
CA2074661A1 (en) 1993-01-27
ES2080432T3 (en) 1996-02-01

Similar Documents

Publication Publication Date Title
EP0525867B1 (en) Two-layer coating systems for wheels and architectural applications
KR930002217B1 (en) Hydroxyalkylamide powder coating composition
CA2012659C (en) Powder paint and a polyester resin for powder paint
EP0107888B2 (en) Polyester and its use in powder coating
CN1033432C (en) Method for preventing filiform corrosion of alumin
CA2156899C (en) Heat curable coating system comprising a plurality of binder resins
CA2485629A1 (en) Low-temperature-curing epoxy-functional powder coating compositions
EP0525870A1 (en) Powder coating composition containing a resin, a curing agent and zinc
CN101200615A (en) Storage-stable powder coating compositions based on polyesters containing acid groups, their production and use thereof
EP1841716A1 (en) Cement-based and fiber cement products
US4463140A (en) Powder coating
US20040236037A1 (en) Particulate coatings having improved chip resistance, UV durability, and color stability
US6011100A (en) Self-Adhesive compositions for coating metal substrates with improved resistance to creep
US4208488A (en) Thermosetting compositions
NZ270274A (en) Thermosetting coating composition comprising linear carboxyl-functional polyester resins, and polyfunctional epoxy compounds and/or beta-hydroxyalkylamides
JPS5998170A (en) Powder paint
JP4035761B2 (en) Resin composition for powder coating, powder coating, and coated body using the same
EP0538931A2 (en) Curing catalyst for the reaction between carboxyl functional polymers and epoxy functional compounds for use in the preparation of powder coatings
JP6178679B2 (en) Railcar exterior with laminated coating
WO1993012157A1 (en) Guanidine catalyst for the reaction between carboxyl functional polymers and epoxy functional compounds as the basis for powder coatings
CA2204936A1 (en) Catalyst for powder coatings
JP2004250628A (en) Powdery coating composition and coated metal article
JPS5829342B2 (en) Resin composition for powder coating
EP0371522A1 (en) Use of a curing catalyst in the preparation of a powder coating composition
JPH1087789A (en) Elastic self-crosslinkable binder for coating can and coil, and its production and use

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE ES FR GB IT NL SE

17P Request for examination filed

Effective date: 19930625

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: AKZO NOBEL N.V.

17Q First examination report despatched

Effective date: 19950127

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE ES FR GB IT NL SE

REF Corresponds to:

Ref document number: 69206509

Country of ref document: DE

Date of ref document: 19960118

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2080432

Country of ref document: ES

Kind code of ref document: T3

ITF It: translation for a ep patent filed

Owner name: BARZANO' E ZANARDO MILANO S.P.A.

ET Fr: translation filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 19960522

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 19960528

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19960603

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 19960610

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19960612

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 19960722

Year of fee payment: 5

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19960730

Year of fee payment: 5

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

26N No opposition filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19970717

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19970718

Ref country code: ES

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 19970718

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19970731

BERE Be: lapsed

Owner name: AKZO NOBEL N.V.

Effective date: 19970731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980201

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 19970717

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980331

NLV4 Nl: lapsed or anulled due to non-payment of the annual fee

Effective date: 19980201

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980401

EUG Se: european patent has lapsed

Ref document number: 92202190.2

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20001204

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20050717